Hand Sanitizer by The Source Design Collections HAND SANITIZER gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by The Source Design Collections. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13%

PURPOSE

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

INACTIVE INGREDIENT

Water (aqua), propylene glycol, phenoxyethanol,fragrance (parfum), hydroxyethylcellulose, alcohol, linalool.

Directions

Place enough product on hands to cover all surfaces.Rub hands together until dry.

WARNINGS

For external use only.

DO NOT USE

Do not use on open skin wounds or children under 2 months of age.

WHEN USING

When using this product keep out of eyes,ears, and mouth. ln case of contact with eyes,rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

Other information

Store in a cool dry place, away from direct sunlight and heat.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81726-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1235 g  in 95 mL

Inactive Ingredients
Ingredient Name	Strength
FRAGRANCE EUCALYPTUS SPEARMINT ORC1601627 (UNII: E90O5M6HMB)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81726-006-01	95 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/12/2021

Labeler - The Source Design Collections (527929622)

Establishment
Name	Address	ID/FEI	Business Operations
The Source Design Collections		527929622	manufacture(81726-006)