BESAFE- hand sanitizer 75% alcohol gel

Besafe by

Drug Labeling and Warnings

Besafe by is a Otc medication manufactured, distributed, or labeled by Zhejiang Guoyao Jingyue Aerosol Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin.

Warnings

For external use only. Flammable, keep away from fire and flame.

DO NOT USE

Do not use in the eyes.

Stop use and ask a doctor if:

• Irritation and redness develop.
• condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DO NOT USE

If swallowed, get medical help or contact a poison control center right away.

Directions

• Wet hands thoroughly with product and allow to dry without wiping.
• for children under 6, use only under adult supervision.
• not recommended for infants.

Other information

Do not store above 105 oF

• May discolor some fabrics
• Harmful to wood finishes & plastic

Inactive Ingredients

Water, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Tocopherol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BESAFE 
hand sanitizer 75% alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75742-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER 940 (UNII: 4Q93RCW27E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75742-011-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
2	NDC: 75742-011-02	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
3	NDC: 75742-011-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
4	NDC: 75742-011-04	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
5	NDC: 75742-011-05	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
6	NDC: 75742-011-06	125 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/07/2020
7	NDC: 75742-011-07	200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020
8	NDC: 75742-011-08	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020
9	NDC: 75742-011-09	375 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020
10	NDC: 75742-011-10	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020
11	NDC: 75742-011-11	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020
12	NDC: 75742-011-12	1200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020
13	NDC: 75742-011-13	1800 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/07/2020

Labeler - Zhejiang Guoyao Jingyue Aerosol Co., Ltd. (554529812)

Registrant - Zhejiang Guoyao Jingyue Aerosol Co., Ltd. (554529812)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.		554529812	manufacture(75742-011)