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Novolin 70/30 by Novo Nordisk

Medically reviewed on January 8, 2018

Dosage form: injection, suspension
Ingredients: INSULIN HUMAN 100[USP'U] in 1mL
Labeler: Novo Nordisk
NDC Code: 0169-1837

Novolin® 70/30, 70% NPH, Human Insulin Isophane Suspension and 30% Regular, Human Insulin Injection (recombinant DNA origin)

PATIENT PACKAGE INSERT
 
70/30 HUMAN Novo Nordisk®

Patient Information for Novolin® 70/30

NOVOLIN® 70/30 (NO-voe-lin)

70% NPH, Human Insulin Isophane Suspension and
30% Regular, Human Insulin Injection
(recombinant DNA origin) 100 units/mL

Important:

Know your insulin. Do not change the type of insulin you use unless told to do so by your healthcare provider. The amount of insulin you take as well as the best time for you to take your insulin may need to change if you take a different type of insulin.

Make sure that you know the type and strength of insulin that is prescribed for you.

Read the Patient Information leaflet that comes with Novolin® 70/30 before you start taking it and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your healthcare provider about your diabetes or your treatment. Make sure you know how to manage your diabetes. Ask your healthcare provider if you have any questions about managing your diabetes.

What is Novolin® 70/30?

Novolin® 70/30 is a man-made insulin (recombinant DNA origin) which is a mixture of 70% NPH, Human Insulin Isophane Suspension and 30% Regular, Human Insulin Injection that is structurally identical to the insulin produced by the human pancreas that is used to control high blood sugar in patients with diabetes mellitus.

Who should not use Novolin® 70/30?

 

Do not take Novolin® 70/30 if:

Your blood sugar is too low (hypoglycemia).
You are allergic to anything in Novolin® 70/30. See the end of this leaflet for a complete list of ingredients in Novolin® 70/30. Check with your healthcare provider if you are not sure.

Tell your healthcare provider:

about all of your medical conditions. Medical conditions can affect your insulin needs and your dose of Novolin® 70/30.
if you are pregnant or breastfeeding. You and your healthcare provider should talk about the best way to manage your diabetes while you are pregnant or breastfeeding. Novolin® 70/30 has not been studied in pregnant or nursing women.
about all of the medicines you take, including prescription and non-prescription medicines, vitamins and herbal supplements. Many medicines can affect your blood sugar levels and your insulin needs. Your Novolin® 70/30 dose may need to change if you take other medicines.
if you take any other medicines, especially ones commonly called TZDs (thiazolidinediones).
if you have heart failure or other heart problems. If you have heart failure, it may get worse while you take TZDs with Novolin® 70/30.

Know the medicines you take. Keep a list of your medicines with you to show all your healthcare providers when you get a new medicine.

How should I take Novolin® 70/30?

To mix Novolin® 70/30, roll gently and use right away. This insulin should not be used if the liquid in the vial remains clear after the vial has been rolled gently. Only use this insulin if it appears cloudy or milky. There may be air bubbles. This is normal. If the precipitate (the white deposit at the bottom of the vial) has become lumpy or granular in appearance or has formed a deposit of solid particles on the wall of the vial, do not use it, and call Novo Nordisk at 1-800-727-6500.

Novolin® 70/30 comes in:

10 mL vials (small bottles) for use with syringe

Read the instructions for use that come with your Novolin® 70/30 product. Talk to your healthcare provider if you have any questions. Your healthcare provider should show you how to inject Novolin® 70/30 before you start taking it. Follow your healthcare provider’s instructions to make changes to your insulin dose.

Take Novolin® 70/30 exactly as prescribed.
Novolin® 70/30 is an intermediate-acting insulin. The effects of Novolin® 70/30 start working ½ hour after injection.
The greatest blood sugar lowering effect is between 2 and 12 hours after the injection. This blood sugar lowering may last up to 24 hours.
While using Novolin® 70/30, any change of insulin should be made cautiously and only under medical supervision. Doses of oral anti-diabetic medicines may also need to change, if your insulin is changed.
Do not mix Novolin® 70/30 with any insulins.
Inject Novolin® 70/30 into the skin of your stomach area, upper arms, buttocks or upper legs. Novolin® 70/30 may affect your blood sugar levels sooner if you inject it into the skin of your stomach area. Never inject Novolin® 70/30 into a vein or into a muscle.
Change (rotate) your injection site within the chosen area (for example, stomach or upper arm) with each dose. Do not inject into the same spot for each injection.
If you take too much Novolin® 70/30, your blood sugar may fall low (hypoglycemia). You can treat mild low blood sugar (hypoglycemia) by drinking or eating something sugary right away (fruit juice, sugar candies, or glucose tablets). It is important to treat low blood sugar (hypoglycemia) right away because it could get worse and you could pass out (become unconscious). If you pass out, you will need help from another person or emergency medical services right away, and will need treatment with a glucagon injection or treatment at a hospital. See “What are the possible side effects of Novolin® 70/30?” for more information on low blood sugar (hypoglycemia).
If you forget to take your dose of Novolin® 70/30, your blood sugar may go too high (hyperglycemia). If  high blood sugar (hyperglycemia) is not treated it can lead to diabetic ketoacidosis, which can lead to serious problems, like loss of consciousness (passing out), coma or even death. Follow your healthcare provider’s instructions for treating high blood sugar (hyperglycemia), and talk to your healthcare provider if high blood sugar is a problem for you. Severe or continuing high blood sugar (hyperglycemia) requires prompt evaluation and treatment by your healthcare provider. Know your symptoms of high blood sugar (hyperglycemia) and diabetic ketoacidosis which may include:
 
increased thirst
frequent urination and dehydration
confusion or drowsiness
loss of appetite
 
fruity smell on breath
high amounts of sugar and ketones in your urine
nausea, vomiting (throwing up) or stomach pain
a hard time breathing

Check your blood sugar levels. Ask your healthcare provider how often you should check your blood sugar levels for hypoglycemia (too low blood sugar) and hyperglycemia (too high blood sugar).

Your insulin dosage may need to change because of:

illness
stress
other medicines you take
change in diet
change in physical activity or exercise
surgery

See the end of this patient information for instructions about preparing and giving the injection.

What should I avoid while using Novolin® 70/30?

Alcohol. Alcohol, including beer and wine, may affect your blood sugar when you take Novolin® 70/30.
Driving and operating machinery. You may have difficulty concentrating or reacting if you have low blood sugar (hypoglycemia). Be careful when you drive a car or operate machinery. Ask your healthcare provider if it is alright to drive if you often have:
low blood sugar
decreased or no warning signs of low blood sugar

What are the possible side effects of Novolin® 70/30?

Low blood sugar (hypoglycemia). Symptoms of hypoglycemia (low blood sugar) may include:
sweating
dizziness or lightheadedness
shakiness
hunger
fast heart beat
tingling of lips and tongue
trouble concentrating or confusion
blurred vision
slurred speech
anxiety, irritability or mood changes
headache

Severe low blood sugar (hypoglycemia) can cause unconsciousness (passing out), seizures, and death. Know your symptoms of low blood sugar. Follow your healthcare provider’s instructions for treating low blood sugar. Talk to your healthcare provider if low blood sugar is a problem for you.

Serious allergic reaction (whole body reaction). Get medical help right away if you develop a rash over your whole body, have trouble breathing, a fast heartbeat, or sweating.
Reactions at the injection site (local allergic reaction). You may get redness, swelling, and itching at the injection site. If you keep having skin reactions, or they are serious, talk to your healthcare provider. You may need to stop using Novolin® 70/30 and use a different insulin. Do not inject insulin into skin that is red, swollen, or itchy.
Skin thickens or pits at the injection site (lipodystrophy). Change (rotate) where you inject your insulin to help prevent these skin changes from happening. Do not inject insulin into this type of skin.
Swelling of your hands and feet
Heart Failure. Taking certain diabetes pills called thiazolidinediones or “TZDs” with Novolin® 70/30 may cause heart failure in some people. This can happen even if you have never had heart failure or heart problems before. If you already have heart failure it may get worse while you take TZDs with Novolin® 70/30. Your healthcare provider should monitor you closely while you are taking TZDs with Novolin® 70/30. Tell your healthcare provider if you have any new or worse symptoms of heart failure including:
shortness of breath
swelling of your ankles or feet
sudden weight gain

Treatment with TZDs and Novolin® 70/30 may need to be adjusted or stopped by your healthcare provider if you have new or worse heart failure.

Vision changes
Low potassium in your blood (hypokalemia)

These are not all of the possible side effects from Novolin® 70/30. Ask your healthcare provider or pharmacist for more information.

 Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

How should I store Novolin® 70/30?

All Unopened Novolin® 70/30:

Keep all unopened Novolin® 70/30 in the refrigerator between 36° to 46°F (2° to 8°C).
Do not freeze. Do not use Novolin® 70/30 if it has been frozen.
If refrigeration is not possible, the unopened vial may be kept at room temperature for up to 6 weeks (42 days), as long as it is kept at or below 77°F (25°C).
Keep unopened Novolin® 70/30 in the carton to protect from light.

Novolin® 70/30 in use:

Vials

Keep at room temperature below 77°F (25°C) for up to 6 weeks (42 days).
Keep vials away from direct heat or light.
Do not refrigerate an opened vial.
Throw away an opened vial after 6 weeks (42 days) of use, even if there is insulin left in the vial.
Unopened vials can be used until the expiration date on the Novolin® 70/30 label, if the medicine has been stored in a refrigerator.

 

General advice about Novolin® 70/30

Novolin® 70/30 is used for the treatment of diabetes only. Medicines are sometimes prescribed for conditions that are not mentioned in the patient leaflet. Do not use Novolin® 70/30 for a condition for which it was not prescribed. Do not give Novolin® 70/30 to other people, even if they have the same symptoms you have. It may harm them.

This leaflet summarizes the most important information about Novolin® 70/30. If you would like more information about Novolin® 70/30 or diabetes, talk with your healthcare provider. For more information, call 1-800-727-6500 or visit www.novonordisk-us.com.

Helpful information for people with diabetes is published by the American Diabetes Association, 1701 N Beauregard Street, Alexandria, VA 22311 and on www.diabetes.org.

Novolin® 70/30 ingredients include:

70% NPH, Human Insulin Isophane Suspension and 30% Regular, Human Insulin Injection (recombinant DNA origin)

Zinc chloride
Sodium hydroxide
Phenol
Disodium phosphate dihydrate
Metacresol
Glycerol
Hydrochloric acid
Protamine sulfate
Water for injections

Date of issue: January 8, 2016

Version: 7

Novolin® and Novo Nordisk® are registered trademarks of Novo Nordisk A/S.

© 2005 - 2016 Novo Nordisk

Manufactured by:

Novo Nordisk A/S

DK-2880 Bagsvaerd, Denmark

For information about Novolin® 70/30 contact:

Novo Nordisk Inc.

800 Scudders Mill Road

Plainsboro, New Jersey 08536

Patient Instructions for Use

Novolin® 70/30 10 mL vial (100 Units/mL, U-100)

Before starting, gather all of the supplies that you will need to use for preparing and giving your insulin injection.

Never re-use syringes and needles.

How should I use the Novolin 70/30 vial?

1.
Check to make sure that you have the correct type of insulin.
2.
Look at the vial and the insulin. The insulin should be a cloudy or milky suspension. The tamper-resistant cap should be in place before the first use. If the cap had been removed before your first use of the vial, or if the precipitate (the white deposit at the bottom of the vial) has become lumpy or granular in appearance or has formed a deposit of solid particles on the wall of the vial, do not use it and call Novo Nordisk at 1-800-727-6500.
3.
Wash your hands with soap and water. If you clean your injection site with an alcohol swab, let the injection site dry before you inject. Talk with your healthcare provider about how to rotate injection sites and how to give an injection.
4.
If you are using a new vial, pull off the tamper-resistant cap. Wipe the rubber stopper with an alcohol swab.
5.
Roll the vial gently 10 times in your hands to mix it. This procedure should be carried out with the vial in a horizontal position. The rolling procedure must be repeated until the suspension appears uniformly white and cloudy. Shaking right before the dose is drawn into the syringe may cause bubbles or froth, which could cause you to draw up the wrong dose of insulin.
6.
Pull back the plunger on the syringe until the black tip reaches the marking for the number of units you will inject.
7.
Push the needle through the rubber stopper of the vial, and push the plunger all the way in to force air into the vial.
8.
Turn the vial and syringe upside down and slowly pull the plunger back to a few units beyond the correct dose.
9.
If there are any air bubbles, tap the syringe gently with your finger to raise the air bubbles to the top. Then slowly push the plunger to the marking for your correct dose. This process should move any air bubbles present in the syringe back into the vial.
10.
Check to make sure you have the right dose of Novolin 70/30 in the syringe.
11.
Pull the syringe with needle out of the vial’s rubber stopper.
12.
Your doctor should tell you if you need to pinch the skin before inserting the needle.  This can vary from patient to patient so it is important to ask your doctor if you did not receive instructions on pinching the skin.  Insert the needle into the skin. Press the plunger of the syringe to inject the insulin. When you are finished injecting the  insulin, pull the needle out of your skin. You may see a drop of Novolin 70/30 at the needle tip. This is normal and has no effect on the dose you just received. If you see blood after you take the needle out of your skin, press the injection site lightly with a piece of gauze or an alcohol wipe. Do not rub the area.
13.
After your injection, do not recap the needle. Place used syringes, needles and used insulin vials in a disposable puncture-resistant sharps container, or some type of hard plastic or metal container with a screw on cap such as a detergent bottle or coffee can.
14.
Ask your healthcare provider about the right way to throw away used syringes and needles. There may be state or local laws about the right way to throw away used syringes and needles. Do not throw away used needles and syringes in household trash or recycle.

Principal Display Panel - 10 mL Vial

NDC 0169-1837-11

Novolin® 70/30 10 mL Vial

70% NPH, Human
Insulin Isophane
Suspension and
30% Regular,
Human Insulin
Injection
(recombinant
DNA origin)

100 units/mL

10 mL

Novo Nordisk®

Principal Display Panel – 10 mL vial ReliOn

NDC 0169-1837-02

Novolin® 70/30

70% NPH, Human Insulin Isophane Suspension
and 30% Regular, Human Insulin Injection
(recombinant DNA origin)

 
100 units/mL 10 mL

ReliOn

NOVOLIN  70/30
human insulin injection, suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0169-1837
Route of AdministrationSUBCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
INSULIN HUMAN (INSULIN HUMAN) INSULIN HUMAN100 [USP'U]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN 
METACRESOL 
PHENOL 
PROTAMINE SULFATE 
SODIUM PHOSPHATE, DIBASIC DIHYDRATE 
ZINC CHLORIDE 
HYDROCHLORIC ACID 
SODIUM HYDROXIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:0169-1837-111 VIAL in 1 CARTON
110 mL in 1 VIAL
2NDC:0169-1837-021 VIAL in 1 CARTON
210 mL in 1 VIAL
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01999106/25/1991
Labeler - Novo Nordisk (622920320)
Establishment
NameAddressID/FEIOperations
Novo Nordisk Pharmaceuticals Industries, Inc.622920320MANUFACTURE(0169-1837)
Establishment
NameAddressID/FEIOperations
Novo Nordisk A/S305914798MANUFACTURE(0169-1837)
Establishment
NameAddressID/FEIOperations
Novo Nordisk A/S305156788API MANUFACTURE(0169-1837)

 
Novo Nordisk

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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