HS HAND SANITIZER- alcohol gel

HS Hand Sanitizer by

Drug Labeling and Warnings

HS Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Nature’s Own Cosmetics Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70% v/v.

Purpose

Antiseptic

Use

Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

Warnings

For external use only.
Flammable. Keep away from open flames and sources of heat.
When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

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

Place product in your palm to thoroughly cover your hand. Rub hands together briskly until dry.
For occasional and personal domestic use.
Supervise children under 6 years of age when using this product.

Other information

Store between 15-30C (59-86F).
Avoid freezing and excessive heat above 40C (104F).
May discolor certain fabrics or surfaces.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Carbomer, dl-alpa Tocopheryl Acetate, Glycerin, lsopropyl Alcohol, Triethanolamine, Water/Aqua/Eau

Questions? 1-800-221-9489

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73756-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73756-003-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/24/2020
2	NDC: 73756-003-02	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/24/2020
3	NDC: 73756-003-03	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/24/2020
4	NDC: 73756-003-04	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/24/2020
5	NDC: 73756-003-05	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/24/2020

Labeler - Nature’s Own Cosmetics Company Inc. (241849371)

Establishment
Name	Address	ID/FEI	Business Operations
Nature’s Own Cosmetics Company Inc.		241849371	manufacture(73756-003)