INSTANT HAND SANITIZER- alcohol gel

INSTANT HAND SANITIZER by

Drug Labeling and Warnings

INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by PERFECT MEDICS, INC, ZHEJIANG RIFESHOW COSMETICS CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antimicrobial

Purpose

Antiseptic

Use

to decrease bacteria on the skin that could cause disease;recommended for repeated use

Warnings

For external use only-hands. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes. In case of contact with eyes flush thoroughly with water;avoid contact with broken skin;do not inhale or ingest
Stop use and ask a doctor if skin irritation develops. 
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

Stop use and ask a doctor if skin irritation develops.

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

• wet hand thoroughly and allow to dry without wiping
• for children under6, use only under adult supervision
• not recommended for infants

Other information

do not store above 105℉;

may discolor some fabrics

harmful to wood finish and plastic

Inactive ingredients

DI water,glycerin, carbopol,triethanolamine,tocopheryl acetate,aloe barbadensis leaf juice

Package Label - Principal Display Panel

Package Label

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79134-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	21.75 mL  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	6.73 mL  in 29 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.29 mL  in 29 mL
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)	0.1015 mL  in 29 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.0725 mL  in 29 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.0029 mL  in 29 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.058 mL  in 29 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79134-005-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
2	NDC: 79134-005-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
3	NDC: 79134-005-03	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/26/2020

Labeler - PERFECT MEDICS, INC (117507545)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG RIFESHOW COSMETICS CO.,LTD		560843477	manufacture(79134-005)