RINSE FREE HAND SANITIZING GEL gel

Rinse Free Hand Sanitizing Gel by

Drug Labeling and Warnings

Rinse Free Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by Guangzhou Qianxiancao Cosmetics Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand sanitizinggel to help reduce bacteria on skin.

Warnings

WarningI This product is for external use and should not be takenorally

2. Use with caution for people with alcohol allergy

3. Keep out of reach of children

4. Highly flammable, keep away from fire and flame

5. Store in a cool, dry placeWhen using this produet, do not use in or near eyes. Incase of contact, rinse eyes thoroughly with water. Stopuse and ask doctor if irritation or rash appears and lastsIf swallowed, get medical help or contact a Poison ControlCenter right away

Do not use

/

WHEN USING

when using this product, do not use in or near eyes. Incase of contact, rinse eyes thoroughly with water. Stopuse and ask doctor if irritation or rash appears and lastsIf swallowed, get medical help or contact a Poison ControlCenter right away.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Direction: Wet and Rub where needed to be sanitizedwith the product thoroughly and allow to dry withoutwiping.

Rinse free.Children under 6 years of age should be supervised whenusing this product.

Other information

• Other information:Store below 106F(41 C)May discolor certain fabric or surfaces

Inactive ingredients

AQUA, 1.3 BUTYLENE GLYCOL, TROLAMINE, CARBOMER.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

RINSE FREE HAND SANITIZING GEL 
rinse free hand sanitizing gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78963-005
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
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78963-005-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 78963-005-05	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 78963-005-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 78963-005-04	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 78963-005-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
6	NDC: 78963-005-06	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
7	NDC: 78963-005-07	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
8	NDC: 78963-005-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
9	NDC: 78963-005-09	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
10	NDC: 78963-005-10	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
11	NDC: 78963-005-11	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
12	NDC: 78963-005-12	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
13	NDC: 78963-005-13	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
14	NDC: 78963-005-14	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
15	NDC: 78963-005-15	10000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
16	NDC: 78963-005-16	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
17	NDC: 78963-005-17	50000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
18	NDC: 78963-005-18	100000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
19	NDC: 78963-005-19	150000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
20	NDC: 78963-005-20	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Guangzhou Qianxiancao Cosmetics Co.,Ltd. (560953777)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Qianxiancao Cosmetics Co.,Ltd.		560953777	manufacture(78963-005)