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allergy relief by McKesson (Sunmark)

Dosage form: capsule
Ingredients: DIPHENHYDRAMINE HYDROCHLORIDE 25mg
Labeler: McKesson (Sunmark)
NDC Code: 70677-0002

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Sunmark 44-190

Active ingredient (in each banded capsule)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses
  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • itchy, watery eyes
    • sneezing
    • itching of the nose or throat
  • temporarily relieves these symptoms due to the common cold:
    • runny nose
    • sneezing

Warnings

Do not use
  • to make a child sleepy
  • with any other product containing diphenhydramine, even one used on skin

Ask a doctor before use if you have
  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product
  • marked drowsiness may occur
  • avoid alcoholic beverages
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • use caution when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions
  • take every 4 to 6 hours
  • do not take more than 6 doses in 24 hours
adults and children 12
years and over
1 to 2 capsules
children 6 to under 12
years
1 capsule
children under 6 years

do not use

Other information
  • TAMPER EVIDENT: PRODUCT SEALED IN PLASTIC STRIPS, CAPSULE BANDED FOR YOUR PROTECTION. DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN OR IF RED BAND AROUND CAPSULE IS BROKEN OR MISSING.
  • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
  • protect from moisture
  • see end flap for expiration date and lot number

Inactive ingredients

butylparaben, corn starch, D&C red #28, edible ink, FD&C blue #1, FD&C red #40, gelatin, lactose anhydrous, magnesium stearate, methylparaben, polysorbate 80, propylparaben, silicon dioxide

Questions or comments?

1-800-426-9391

Principal display panel

 sunmark®

COMPARE TO BENADRYL®
ACTIVE INGREDIENT*
NDC 70677-0002-1

allergy relief
DIPHENHYDRAMINE HCl, 25 mg
Antihistamine

relieves
sneezing,
runny nose,
itchy, watery eyes,
itchy throat

24 CAPSULES

TAMPER EVIDENT: PRODUCT SEALED IN PLASTIC STRIPS,
CAPSULE BANDED FOR YOUR PROTECTION. DO NOT USE IF
BLISTER UNIT IS TORN OR BROKEN OR IF RED BAND
AROUND CAPSULE IS BROKEN OR MISSING.

*This product is not manufactured or distributed by Johnson
& Johnson Corporation, owner of the registered trademark Benadryl®.
50844           REV1016A19008

Another Quality Product
Distributed by McKesson
One Post Street, San Francisco, CA 94104
Money Back Guarantee
Please visit us at www.sunmarkbrand.com

Sunmark 44-190

ALLERGY RELIEF 
diphenhydramine hcl capsule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70677-0002
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
BUTYLPARABEN 
STARCH, CORN 
D&C RED NO. 28 
FD&C BLUE NO. 1 
FD&C RED NO. 40 
GELATIN, UNSPECIFIED 
ANHYDROUS LACTOSE 
MAGNESIUM STEARATE 
METHYLPARABEN 
POLYSORBATE 80 
PROPYLPARABEN 
SILICON DIOXIDE 
Product Characteristics
ColorPINK, WHITEScoreno score
ShapeCAPSULESize14mm
FlavorImprint Code44;107
Contains    
Packaging
#Item CodePackage Description
1NDC:70677-0002-12 BLISTER PACK in 1 CARTON
112 CAPSULE in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34103/15/1990
Labeler - McKesson (Sunmark) (177667227)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(70677-0002)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(70677-0002)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088MANUFACTURE(70677-0002), PACK(70677-0002)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(70677-0002)

 
McKesson (Sunmark)

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Medically reviewed on Oct 15, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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