ISOPROPYL ALCOHOL 91 PERCENT- isopropyl alcohol liquid

Isopropyl Alcohol 91 Percent by

Drug Labeling and Warnings

Isopropyl Alcohol 91 Percent by is a Otc medication manufactured, distributed, or labeled by Humco Holding Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Isopropyl Alcohol 91% 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

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

Inactive Ingredient

purified water

Good Neighbor Label

Health Mart Label

Sunmark Label

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 91 PERCENT 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0395-9119
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	910 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: 0395-9119-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2016

Labeler - Humco Holding Group, Inc. (825672884)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	analysis(0395-9119) , manufacture(0395-9119) , pack(0395-9119) , label(0395-9119)