NO-WASH ANTIBACTERIAL WASH HAND gel

NO-WASH ANTIBACTERIAL WASH HAND by

Drug Labeling and Warnings

NO-WASH ANTIBACTERIAL WASH HAND by is a Otc medication manufactured, distributed, or labeled by Guangdong Boxi High-tech Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75%,Chloroxylenol 0.05%

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on skin

WARNINGS

For external use only. Flammable. Keep away from heat or flame

When using this product

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

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 15-30'C(59-86 F)

INACTIVE INGREDIENTS

Water(Aqua), Fragrance, Carbomer, Triethanolamine, CI 42053

DO NOT USE

STOP USE

KEEP OUT OF REACH OF CHILDREN

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

NO-WASH ANTIBACTERIAL WASH HAND 
no-wash antibacterial wash hand gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75702-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.05 g  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
TROLAMINE (UNII: 9O3K93S3TK)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CARBOMER 934 (UNII: Z135WT9208)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75702-007-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
2	NDC: 75702-007-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
3	NDC: 75702-007-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
4	NDC: 75702-007-04	68 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
5	NDC: 75702-007-05	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
6	NDC: 75702-007-06	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
7	NDC: 75702-007-07	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
8	NDC: 75702-007-08	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
9	NDC: 75702-007-09	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
10	NDC: 75702-007-10	280 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
11	NDC: 75702-007-11	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
12	NDC: 75702-007-12	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
13	NDC: 75702-007-13	600 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
14	NDC: 75702-007-14	800 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
15	NDC: 75702-007-15	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
16	NDC: 75702-007-16	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
17	NDC: 75702-007-17	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
18	NDC: 75702-007-18	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
19	NDC: 75702-007-19	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020

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

Labeler - Guangdong Boxi High-tech Co.,Ltd. (542874709)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Boxi High-tech Co.,Ltd.		542874709	manufacture(75702-007)