Drug Facts

Active Ingredient

Isopropyl Alcohol 70% by volume

Purpose

First aid antiseptic

Use

First aid to help prevent the risk of infection in.

minor cuts
scrapes
burns

Warnings

For external use only.

Flammable, keep way from spark, heat and flame.
Use in well ventilated area, fumes may be harmful.

Ask a doctor before use for

deep wounds
animal bites
serious burns

When using this product

do not get into eyes or mucous membranes.
do not apply to irritated skin.

Stop use and ask a doctor if

excessive irritation of the skin develops.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

apply freely and rub briskly with hands or towel.

Other Information

does not contain ethyl or grain alcohol and is not sold as a substitute for preparations containing the same.
Store at controlled room temperature
will produce serious gastric disturbances if taken internally.

Inactive Ingredient

Methyl salicylate 0.5%

FDC Blue #1

FDC Yellow #5

purified water

Principal Display Panel

NDC 46122-331-43

ISOPROPYL

RUBBING

ALCOHOL 7 0%

With Wintergreen Oil

Rubbing, Massage, Sponge Bath

16 fl oz (1 pt) 473 mL

Principal Display Panel
NDC 46122-331-43
ISOPROPYL
RUBBING
ALCOHOL 70%
With Wintergreen Oil
Rubbing, Massage, Sponge Bath
16 fl oz (1 pt) 473 mL

GNP ISOPROPYL ALCOHOL 70 PERCENT WITH WINTERGREEN OIL
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:46122-331
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	700 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
METHYL SALICYLATE (UNII: LAV5U5022Y)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:46122-331-43	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	01/01/2016

Labeler - Amerisource Bergen (007914906)

Registrant - Pharma Nobis, LLC (118564114)

Name	Address	ID/FEI	Business Operations
Establishment
Pharma Nobis, LLC		118564114	analysis(46122-331) , manufacture(46122-331) , pack(46122-331) , label(46122-331)

GNP Isopropyl Alcohol 70 Percent USP With Wintergreen Oil