UP AND UP ALCOHOL- isopropyl alcohol swab

Up and Up alcohol by

Drug Labeling and Warnings

Up and Up alcohol by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

UP AND UP ALCOHOL 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-809
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-809-30	100 in 1 BOX
1	NDC: 11673-809-09	1 in 1 PACKET
1		5 mL in 1 APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2010

Labeler - Target Corporation (006961700)