75% ALCOHOL INSTANT HAND SANITIZER gel

75% Alcohol Instant Hand Sanitizer by

Drug Labeling and Warnings

75% Alcohol Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by FEEL LIFE CO.,LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 75%

Purpose

Antiseptic

Uses

To decrease bacteria on the skin.Recommended for repeated use.

Warnings

Keep away from fire or flame.

For external use only:Hands

DO NOT USE

When using this product

Do not use in or around 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.

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

1.Place enough product in you palm to thoroughly spread on both hands

and rub into the skin until dry.

2.Children under 6 years of age should be supervised when using this product.

Other information

1.Store below 106°F(41℃)

2.May discolor certain fabrics or surfaces

Inactive ingredients

Water、Carbomer、Triethanolamine、Lavander oil.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

75% ALCOHOL INSTANT HAND SANITIZER 
75% alcohol instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75879-001
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75879-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
2	NDC: 75879-001-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
3	NDC: 75879-001-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
4	NDC: 75879-001-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
5	NDC: 75879-001-05	119 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
6	NDC: 75879-001-06	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
7	NDC: 75879-001-07	149 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
8	NDC: 75879-001-08	199 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
9	NDC: 75879-001-09	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
10	NDC: 75879-001-10	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
11	NDC: 75879-001-11	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
12	NDC: 75879-001-12	349 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
13	NDC: 75879-001-13	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
14	NDC: 75879-001-14	499 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
15	NDC: 75879-001-15	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020
16	NDC: 75879-001-16	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/11/2020

Labeler - FEEL LIFE CO.,LIMITED (421264782)

Registrant - FEEL LIFE CO.,LIMITED (421264782)

Establishment
Name	Address	ID/FEI	Business Operations
FEEL LIFE CO.,LIMITED		421264782	manufacture(75879-001)