RUBBING ALCOHOL- isopropyl alcohol solution

Rubbing Alcohol by

Drug Labeling and Warnings

Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Super Dope Laboratories LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl Alcohol 99% v/v. Purpose: Antiseptic

Purpose

Antiseptic

Use

For first aid use to decrease germs in minor cuts and scrapes

Warnings

For external use only.
If taken internally serious gastric disturbances will result
Do not use in or near the eyes
In case of deep or puncture wounds, consult your doctor.
Flammable keep away from heat or flame.
Use only in a well-ventilated area; fumes may be toxic.
Ask a doctor before use if you have deep or puncture wounds, animal
bites or serious burns.

WHEN USING

When using this product
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

Keep out of reach of children. In case of ingestion, get medical help
or contact a Poison Control Center immediately.

Directions

• Directions Clean affected area Apply a small amount of this product
  1-3 times daily If bandaged let dry first May be covered with a sterile
  bandage

Other information

• Other information
  Store at room temperature
  Does not contain, nor is intended as a substitute for ethyl alcohol

Inactive ingredients

Inactive Ingredients: Purified Water.

Package Label - Principal Display Panel

3785mL NDC: 74220-006-01

INGREDIENTS AND APPEARANCE

RUBBING ALCOHOL 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74220-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	99 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: 74220-006-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/31/2020

Labeler - Super Dope Laboratories LLC (055650002)

Establishment
Name	Address	ID/FEI	Business Operations
Super Dope Laboratories LLC		055650002	manufacture(74220-006) , label(74220-006)