RUBBING ALCOHOL- isopropyl alcohol liquid

Rubbing Alcohol by

Drug Labeling and Warnings

Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Nobum Labs, S.A.P.I. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl Alcohol 70% v/v. Purpose: First Aid Antiseptic

Purpose

First Aid Antiseptic

Use

First aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

Keep away from heat or flame. If taken internally serious gastric disturbances will result.

ASK DOCTOR

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns.

WHEN USING

* do not get into eyes.

* do not apply over large areas of the body.
*do not use longer than one week unless directed by a doctor.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

In case of ingestion, get medical help or call Poison Control Center immediately.

Directions

* clean affected area

*apply small amount of this product on the area 1-3 times daily

* If bandaged, lets dry first may be covered with a sterile bandage

Other information

store at room temperature does not contain, nor is intended as a sustitute for grain or ethyl alcohol.

Inactive ingredients

purified water.

Package Label - Principal Display Panel 500 ml NDC:

81213-001-01

500 ml NDC: 81213-001-01

946 mL NDC:

81213-001-02

946 mL NDC: 81213-001-02

INGREDIENTS AND APPEARANCE

RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81213-001
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)	30 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81213-001-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/24/2022
2	NDC: 81213-001-02	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/24/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/24/2022

Labeler - Nobum Labs, S.A.P.I. de C.V. (951588419)

Registrant - Nobum Labs, S.A.P.I. de C.V. (951588419)

Establishment
Name	Address	ID/FEI	Business Operations
Nobum Labs, S.A.P.I. de C.V.		951588419	manufacture(81213-001)