HUMCO ISOPROPYL RUBBING ALCOHOL 70%- isopropyl alcohol liquid

HUMCO Isopropyl Rubbing Alcohol 70% by

Drug Labeling and Warnings

HUMCO Isopropyl Rubbing Alcohol 70% by is a Otc medication manufactured, distributed, or labeled by Humco Holding Group, Inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

Ask a doctor before use for

• deep wounds
• animal bites
• serious burns

When using this product

• do not get into eyes
• do not apply over large areas of the body
• do not use longer than 1 week

Stop use and ask a doctor if

condition persists or gets worse

Keep out of reach of children.

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

Directions

• clean the affected area.
• apply a smal amount of this product on the affected area 1 to 3 times daily.
• may be covered with sterile bandage.
• if bandaged, let it dry first.

Other Information

• store at room temperature
• does not contain, nor is intended as a substitute for grain or ethyl alcohol.
• will produce serious gastric distrurbances if taken internally.

Inactive Ingredient

purified water

Principal Display Panel

INGREDIENTS AND APPEARANCE

HUMCO ISOPROPYL RUBBING ALCOHOL 70% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-1249
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0395-1249-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/14/2017
2	NDC: 0395-1249-28	3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/14/2017
3	NDC: 0395-1249-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2008

Labeler - Humco Holding Group, Inc. (825672884)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	manufacture(0395-1249) , analysis(0395-1249) , pack(0395-1249) , label(0395-1249)