DOP ISOPROPYL RUBBING ALCOHOL 70%- isopropyl alcohol liquid

DOP Isopropyl Rubbing Alcohol 70% by

Drug Labeling and Warnings

DOP Isopropyl Rubbing Alcohol 70% by is a Otc medication manufactured, distributed, or labeled by Omega & Delta Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 70%

Purpose

First aid antiseptic

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Use helps prevent the risk of infection in minor cuts, scrapes and burns

WARNINGS

Warnings  For external use only

Flammable keep away from fire or flame, heat, spark, electrical

Ask a doctor before use for deep wounds, animal bites or serious burns

When using this product do not get into eyes do not apply over large area of the body do not use longer than 1 week

Stop use and ask a doctor if the condition persists or gets worse

DOSAGE & ADMINISTRATION

Directions clean the affected area apply 1 to 3 times daily

INACTIVE INGREDIENT

Inactive ingredient Purified water

OTHER SAFETY INFORMATION

Other information does not contain, nor is intended as a substitute for grain or ethyl alcohol will produce serious gastric disturbances if taken internally

SPL UNCLASSIFIED SECTION

Manufactured by:

Omega & Delta Co., Inc.

Carolina, P.R. 00984

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOP ISOPROPYL RUBBING ALCOHOL 70% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51048-005
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: 51048-005-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2000
2	NDC: 51048-005-32	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2000

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2000

Labeler - Omega & Delta Co., Inc. (090317793)

Establishment
Name	Address	ID/FEI	Business Operations
Omega & Delta Co., Inc.		090317793	manufacture(51048-005)