ADVANCE HAND SANITIZER gel

Advance Hand Sanitizer by

Drug Labeling and Warnings

Advance Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Youxing Cosmetics CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl alcohol 75% V/V

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. 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, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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. If swallowed, get medical help or contact a Poison Control Center 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

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water(Aqua). Aloe Barbadensis Leaf Juice,Carbomer, Fragrance. Glycerin,Propylene Glycol ,Tocopheryl Acetate(Vitamin E).Triethanolamine, FD&C Blue No 1. FD&C Yellow No 5

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ADVANCE HAND SANITIZER 
advance hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75239-005
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
GLYCERIN (UNII: PDC6A3C0OX)	1 g  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 g  in 100 mL
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)	0.05 g  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.5 g  in 100 mL
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.05 g  in 100 mL
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)	0.05 g  in 100 mL
CARBOMER 934 (UNII: Z135WT9208)	1 g  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.3 g  in 100 mL
BENZYL ALCOHOL (UNII: LKG8494WBH)	0.05 g  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75239-005-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
2	NDC: 75239-005-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
3	NDC: 75239-005-03	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
4	NDC: 75239-005-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
5	NDC: 75239-005-05	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
6	NDC: 75239-005-06	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
7	NDC: 75239-005-07	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
8	NDC: 75239-005-08	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
9	NDC: 75239-005-09	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
10	NDC: 75239-005-10	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
11	NDC: 75239-005-11	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
12	NDC: 75239-005-12	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
13	NDC: 75239-005-13	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
14	NDC: 75239-005-14	650 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
15	NDC: 75239-005-15	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
16	NDC: 75239-005-16	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020
17	NDC: 75239-005-17	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/21/2020

Labeler - Guangzhou Youxing Cosmetics CO.,LTD (544355953)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Youxing Cosmetics CO.,LTD		544355953	manufacture(75239-005)