RUBBING ALCOHOL 50%- isopropyl alcohol liquid

RUBBING ALCOHOL 50% by

Drug Labeling and Warnings

RUBBING ALCOHOL 50% by is a Otc medication manufactured, distributed, or labeled by HIND PHARMA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts:

Active ingredients:

Isopropyl alcohol 50% concentrate 

PURPOSE

for antimicrobial topical use.

Uses:

As a first aid to help prevent the risk of infection in minor cuts, scrapes & burns.

Warning:

Flammable!

1. Keep the product away from direct sunlight, heat, flame/fire, spark and electricity.
2. Do not use as a substitute of ethyl alcohol or grain.
3. Not for medicinal use
4. Pregnant or nursing mothers must prefer consulting the doctor before usage.
5. For external use only. Stop using if any irritation/ Pin or swelling occurs.

Emergency/ First aid:

In case of direct contact of;

Eyes: Wash the eyes with fresh water for 25 minutes and seek medical assistance. 

Skin: Wash with soap and water. Consult doctor if irritation persists.

Inhalation: Move to fresh air

Keep away from children. In case of accidental ingestion, seek assistance or rush to Poison control center immediately.

Direction:

1. Use a clean swab, cotton or gauze to apply on the skin directly.
2. Use clean hands for the purpose of rubbing.

Inactive ingredients:

Purified water

SPL UNCLASSIFIED SECTION

Clean/ Sparkle/Hygenic

FIRST AID ANTISEPTIC For Rubbing & Massaging

Use only in a well ventilated area. Fumes may be harmful.

Manufactured by: 

HIND PHARMA

11-G, J.K. Road, Industrial Area, Govindpura, Bhopal, M.P., INDIA-462022

Packaging

INGREDIENTS AND APPEARANCE

RUBBING ALCOHOL 50% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73592-050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	50 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: 73592-050-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/05/2020

Labeler - HIND PHARMA (871384791)

Establishment
Name	Address	ID/FEI	Business Operations
HIND PHARMA		871384791	manufacture(73592-050)