SCENTED HAND SANITIZER gel

Scented Hand Sanitizer by

Drug Labeling and Warnings

Scented Hand 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

Hand sanitizer to help decrease bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

■ For external use only.

■ When using this product do notuse in or near the eyes. In case of contact, rinse eyes thoroughly with water.

■ Stop use andask 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

■ 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

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

Other

■ Store at room temperature

■ May discolor certain fabrics or surfaces

Principal Display Panel

INGREDIENTS AND APPEARANCE

SCENTED HAND SANITIZER 
scented hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-608
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
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-608-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
2	NDC: 70445-608-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
3	NDC: 70445-608-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
4	NDC: 70445-608-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
5	NDC: 70445-608-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
6	NDC: 70445-608-06	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/20/2024
7	NDC: 70445-608-07	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/20/2024
8	NDC: 70445-608-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/20/2024
9	NDC: 70445-608-09	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(70445-608)