Unscented Sanitizer by Beacon Promotions, Inc. UNSCENTED SANITIZER gel

Unscented Sanitizer by

Drug Labeling and Warnings

Unscented Sanitizer by is a Otc medication manufactured, distributed, or labeled by Beacon Promotions, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Ethyl alcohol 63.5%

Put enough product in your palm to cover your hands and rub together briskly until dry

Purpose

Antimicrobial

Use

Antimicrobial

Warnings

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 a doctor if irritation or rash appears and lasts.

■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep Out of Reach of Children

Keep Out of Reach of Children

Directions

Directions

■ Put enough product in your palm to cover your hands and rub together briskly until dry

■ Children under 6 years of age should be supervised when using this product

Drug Facts

Ethyl alcohol 63.5% w/w

Inactive Ingredients

Inactive ingredients: Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/ VP Copolymer Hydroxypropyl Methylcellulose, Mannitol, Microcrystalline Cellulose, Propylene Glycol, Aqua, Tocopheryl Acetate

Other Information

■ Store at room temperature

■ May discolor certain fabrics or surfaces

Principal Display Panel

INGREDIENTS AND APPEARANCE

UNSCENTED SANITIZER 
unscented sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-609
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-609-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
2	NDC: 70445-609-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
3	NDC: 70445-609-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
4	NDC: 70445-609-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
5	NDC: 70445-609-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
6	NDC: 70445-609-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/20/2024
7	NDC: 70445-609-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/20/2024
8	NDC: 70445-609-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
9	NDC: 70445-609-09	480 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/20/2024

Labeler - Beacon Promotions, Inc. (119056382)

Establishment
Name	Address	ID/FEI	Business Operations
Beacon Promotions, Inc.		119056382	manufacture(70445-609)