BODY WIPE by ZheJiang HuaShun Technology Co.,Ltd BODY WIPE- wipe patch

BODY WIPE by

Drug Labeling and Warnings

BODY WIPE by is a Otc medication manufactured, distributed, or labeled by ZheJiang HuaShun Technology Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium chloride 0.13%. Purpose: Antimicrobial

Purpose

Antimicrobial, wipe

Use

decrease bacteria on the skin

Warnings

For external use only.

Do not use

if you are allergic to any of the ingredients.

WHEN USING

When using this product avoid contact with eyes.if contact occurs,rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.

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 appear

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

to maximize efectiveness,use a different side on each body part.Allow skin to air dry.Do not flush.

Inactive ingredients

water,aloe barbadensis leaf juice,citric acid，fragrance,glycerin,hamamelis virginiana(witch hazel) bark/leaf/twig extract,phenoxyethanol,polysibate 20,tocopheryl acetate.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

BODY WIPE 
wipe patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77046-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.039 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)	0.015 g  in 30 g
ALOE (UNII: V5VD430YW9)	0.015 g  in 30 g
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.15 g  in 30 g
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.015 g  in 30 g
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.045 g  in 30 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77046-005-01	10 in 1 BOX	07/13/2020
1		30 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/13/2020

Labeler - ZheJiang HuaShun Technology Co.,Ltd (527157837)

Establishment
Name	Address	ID/FEI	Business Operations
ZheJiang HuaShun Technology Co.,Ltd		527157837	manufacture(77046-005)