PREMIER INSTANT- alcohol 80% liquid

PREMIER INSTANT by

Drug Labeling and Warnings

PREMIER INSTANT 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 80%, USP

Purpose

Antimicrobial

Uses

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 eyes thoroughly with water

Stop use and ask doctor if

irritation or rash appears and lasts

Keep out of reach of children.

If swallowed, get medical help right away or contact a Poison Control Center immediately.

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• 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 this PREMIER PURE

Other information

• Store below 1100 F (430C)
•  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 ingredient

Water(DI), Glycerin, Text-butyl Alcohol, Denatonium Bezoate

Pricipal Display Panel 

INGREDIENTS AND APPEARANCE

PREMIER INSTANT 
alcohol 80% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73945-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73945-001-01	59.14 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
2	NDC: 73945-001-02	236.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
3	NDC: 73945-001-03	443.6 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
4	NDC: 73945-001-04	946.3 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
5	NDC: 73945-001-05	2011 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	03/23/2020

Labeler - RPP PRODUCTS, INC. (623623852)

Establishment
Name	Address	ID/FEI	Business Operations
RPP PRODUCTS, INC.		623623852	manufacture(73945-001)