WET WIPES- salicylic acid swab

wet wipes by

Drug Labeling and Warnings

wet wipes by is a Otc medication manufactured, distributed, or labeled by HANGZHOU GUOGUANG TOURING COMMODITY CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

salicylic acid 0.5%

Purpose

acne treatment

Use

for the treatment of acne

Warnings

for external use only
when using this product
with other topical acne medications ,at the same time or immediately afterwards ,increased skin dryness ,redness or
irritation may occur .If this happens ,only one medication should be used unless directed by a doctor.
avoid contact with eyes .if contact occurs, rinse thoroughly with water. keep away from mouth and lips.
stop use and ask doctor if skin irritation occurs.
Keep out of reach of children ,If swallowed ,get medical help or contact a Poison Control Center immediately.

Keep out of reach of children

Keep out of reach of children ,If swallowed ,get medical help or contact a Poison Control Center immediately.

Directions

cleanse skin thoroughly before applying medication ,remove wipe ,unfold and wipe over entire affected area.
reseal label on package to maintain freshness.

INACTIVE INGREDIENT

aqua (water),glycerin, propylene glycol , dodecyl polyglucoside, polysorbate 20,HEXYLENE GLYCOL , BENZYL ALCOHOL ,SODIUM LAURAMINOPROPIONATE ,ALOE BARBADENSIS(ALOE VERA )EXTRACT ,WHITE TEA EXTRACT ,CHAMOMILLA RECUTITA(CHAMOMILE)EXTRACT ,GLYDANT DMDM H,PHENOXYETHANOL ,PEG-40 HYDROGENATED CASTOR OIL,TOCOPHERYL ACETATE(VITAMIN E) ,DISODIUM EDTA,IODOPROPYNYL BUTYLCARBAMATE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WET WIPES 
salicylic acid swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61312-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DODECYL PROPIONATE (UNII: 7G537BMD9L)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM LAURAMINOPROPIONATE (UNII: X5NJA9HXPU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TEA LEAF OIL (UNII: VC855RRT77)
CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PEG-40 HYDROGENATED LANOLIN (UNII: 959P5CXE48)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61312-004-01	35 in 1 BAG	01/01/2018
1		0.00054 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	02/25/2015

Labeler - HANGZHOU GUOGUANG TOURING COMMODITY CO., LTD. (526890634)

Establishment
Name	Address	ID/FEI	Business Operations
HANGZHOU GUOGUANG TOURING COMMODITY CO., LTD.		526890634	manufacture(61312-004)