INSTANT HAND SANITIZER gel

INSTANT HAND SANITIZER by

Drug Labeling and Warnings

INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Double Body Biotech Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on skin.

WARNINGS

Flammable, Keep away from fire or flame.
For external use only.

DO NOT USE

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 doctor if irritation or rash appears and lasts. Keep out of reach for children. If swallowed, get

medical help or contact a Poison Control Center right away.

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.

Other Information

Store below 106° F.(41℃)

INACTIVE INGREDIENTS

Alcohol, Aqua, Glycereth-26, Aloe Barbadensis Leaf Extract,Carbomer,Sodium Hydroxide.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74657-001
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
GLYCERETH-26 (UNII: NNE56F2N14)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74657-001-01	29.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
2	NDC: 74657-001-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
3	NDC: 74657-001-03	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
4	NDC: 74657-001-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
5	NDC: 74657-001-05	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
6	NDC: 74657-001-06	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
7	NDC: 74657-001-07	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
8	NDC: 74657-001-08	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
9	NDC: 74657-001-09	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
10	NDC: 74657-001-10	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
11	NDC: 74657-001-11	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
12	NDC: 74657-001-12	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Double Body Biotech Limited (560246954)

Registrant - Double Body Biotech Limited (560246954)

Establishment
Name	Address	ID/FEI	Business Operations
Double Body Biotech Limited		560246954	manufacture(74657-001)