ISOPROPYL ALCOHOL 99 PERCENT- isopropyl alcohol liquid

Isopropyl Alcohol 99 Percent by

Drug Labeling and Warnings

Isopropyl Alcohol 99 Percent by is a Otc medication manufactured, distributed, or labeled by All Pharma LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol 99% 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 inhale

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 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.

Inactive Ingredient

purified water

Principal Display Panel

ISOPROPYL
RUBBING
ALCOHOL 99%
USP
First Aid Antiseptic
NDC: 53149-1111-1 Bottle of 16 fl oz (1 pt) 473 mL
NDC: 53149-1111-3 Bottle of 32 fl oz (1 qt) 946 mL
NDC: 53149-1111-5 Bottle of 128 fl oz (1 Gallon) 3.79 L

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 99 PERCENT 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53149-1111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	990 mg  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53149-1111-1	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020
2	NDC: 53149-1111-3	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020
3	NDC: 53149-1111-5	3790 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2020

Labeler - All Pharma LLC (117605075)

Registrant - All Pharma LLC (117605075)

Establishment
Name	Address	ID/FEI	Business Operations
All Pharma LLC		117605075	manufacture(53149-1111)