ALCOHOL FREE- alcohol free spray spray

Alcohol Free by

Drug Labeling and Warnings

Alcohol Free by is a Otc medication manufactured, distributed, or labeled by Collective Science Integration, P&P International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

INACTIVE INGREDIENT

INDICATIONS & USAGE

ACTIVE INGREDIENT

KEEP OUT OF REACH OF CHILDREN

PURPOSE

WARNINGS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOHOL FREE 
alcohol free spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90055-216
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 0.13 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90055-216-16	472 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/18/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/18/2021

Labeler - Collective Science Integration (133591508)

Establishment
Name	Address	ID/FEI	Business Operations
P&P International		133591508	manufacture(90055-216)