HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Biolab International Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Ethyl Alcohol 62%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

Uses hand sanitizer to help reduce bacteria on the skin . For occassional and personal domestic use

WARNINGS

Warnings

for external use only: hands

Flammable. Keep away from fire or flame

WHEN USING

when using this product, avoid contact with eyes, in case of contact, rinse eyes thoroughly with water, avoid contact with broken skin .

STOP USE

Stop use and consult a doctor if . irritation or redness develops. condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. children under 6, use only under adult supervision, Not recommended for infants.

For external use only. Do not drink.
If swallowed, seek professional assistance or contact a poison control center.

DOSAGE & ADMINISTRATION

Directions. Place enough product in your palm to thoroughly spread on both hands and rub into skin until dry.

STORAGE AND HANDLING

Other information. do not store above 105°F， may discolor some fabics. harmful to wood finished and plastics

INACTIVE INGREDIENT

Inactive ingredients acrylates/C10-C30 alkyl acrylate crosspolymer,aloe barbadensis leaf juice, glycerin, maltodextrin, propylene glycol, water , triethanolamine,Fragrance. FD&C Blue No.1, FD&C Yellow No.5

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72264-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72264-008-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/29/2020

Labeler - Biolab International Incorporated (200167919)