PREMIER PURE PROTECTION- alcohol gel

Premier Pure Protection by

Drug Labeling and Warnings

Premier Pure Protection by is a Otc medication manufactured, distributed, or labeled by RPP Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 72% v/v.

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from fire or flame

For external use only.

When using this product do not use in or near the eyes.In case of contact rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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.

Directions

• Put enough product in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using PREMIER PURE.

Other information

• Store below 110º F (43º C).
• May discolor certain fabrics or surfaces.
• This product does not contain any chemicals known to the State of California to cause cancer, birth defects, or any other reproductive harm.

Inactive ingredients

Water, Acrylates Copolymer, Glycerin, Hydrolyzed Jojoba Esters, Aminomethyl Propanol, Fragrance

Product Label

INGREDIENTS AND APPEARANCE

PREMIER PURE PROTECTION 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73945-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS) (UNII: CH428W5O62)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73945-005-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
2	NDC: 73945-005-02	89 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
3	NDC: 73945-005-03	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
4	NDC: 73945-005-04	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
5	NDC: 73945-005-05	1893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
6	NDC: 73945-005-06	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/08/2020

Labeler - RPP Products, Inc. (623623852)