HAND SANITIZER- alcohol hand sanitizer gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ningbo Lanzi Cosmetic Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 68% w/w. Purpose: Antiseptic

Purpose

Antiseptic

Use

For hand sanitizing to reduce bacteria on the skin.

Warnings

Flammable.

Keep away from fire or flame.

For external use only.

Do not inhale or ingest.

Do not use

Do not inhale or ingest.

WHEN USING

When using this product Keep out of eyes.

In case of contact, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash appears or lasts.

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

Squeeze out enough product in your palm to cover hands and rub hands together briskly until dry.

Other information

Store below 110℉ (43℃).

Inactive ingredients

Ethyl Alcohol, Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium EDTA, Tocopheryl Acetate, Deionized Water.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75613-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CLOVE (UNII: K48IKT5321)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75613-101-21	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
2	NDC: 75613-101-22	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
3	NDC: 75613-101-30	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
4	NDC: 75613-101-31	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
5	NDC: 75613-101-32	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
6	NDC: 75613-101-33	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
7	NDC: 75613-101-71	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
8	NDC: 75613-101-72	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
9	NDC: 75613-101-75	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
10	NDC: 75613-101-76	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
11	NDC: 75613-101-77	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020
12	NDC: 75613-101-79	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/27/2020

Labeler - Ningbo Lanzi Cosmetic Technology Co., Ltd (554530929)

Registrant - A03 Lab of BTS (548009541)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Lanzi Cosmetic Technology Co., Ltd		554530929	manufacture(75613-101) , label(75613-101)