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Up and Up alcohol

Dosage form: swab
Ingredients: ISOPROPYL ALCOHOL 70mL in 100mL
Labeler: Target Corporation
NDC Code: 11673-809

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.

Drug Facts

Active ingredient

Isopropyl alcohol, 70% v/v

Purpose

Antiseptic

Uses
for preparation of the skin prior to injection
first aid to decrease germs in minor cuts, scrapes and burns

Warnings

For external use only.

When using this product
do not get into eyes
do not apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask a doctor if

condition persists or gets worse or lasts for more than 72 hours. Do not use longer than 1 week unless directed by a doctor.

Flammable, keep away from fire or flame.
Do not use with electrocautery procedures
Use only in a well ventilated area; fumes may be toxic.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to skin as needed. Discard after single use.

Other information

Protect from freezing and avoid excessive heat

Inactive ingredients

Water

Package/Label Principal Display Panel

Up&Up

alcohol swabs

70% isopropyl alcohol

sterile

antiseptic for preparation of skin prior to injection

2-ply swabs

individually wrapped

100 COUNT

100 PADS – 1 1/8 in x 2 3/8 in (2.8 cm x 6 cm)

Package/Label Back

Alcohol Swabs back

UP AND UP ALCOHOL 
isopropyl alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-809
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:11673-809-30100 PACKET in 1 BOX
1NDC:11673-809-091 APPLICATOR in 1 PACKET
15 mL in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2010
Labeler - Target Corporation (006961700)

 
Target Corporation

Medically reviewed on Dec 26, 2017

Further information

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

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