ACNE TREATMENT- salicylic acid cream

ACNE TREATMENT by

Drug Labeling and Warnings

ACNE TREATMENT by is a Otc medication manufactured, distributed, or labeled by COB Ecommerce Empire LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic acid 0.5%

Purpose

Acne treatment

Use

For the treatment of acne.

Warnings

For external use only.

When using this product

• skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Keep out of reach of children.

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

Directions

• clean the skin thoroughly before applying this product
• cover the entire affected area with a thin layer one to three times daily
• because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Inactive ingredients

deionized water, stearic acid, glyceryl stearate, shea butter, rosehips seed oil, sesame seed oil, olive oil, white willow extract, burdock extract, milk thistle extract, hops extract, sophora root extract, squalene, isooctyl palmitate, isopropyl myristate, polydimethylsiloxane, tocopherol, tea tree oil, phenoxyethanol, DL-menthol, hyaluronic acid, grape seed extract

ACNE TREATMENT CREAM SALICYLIC ACID, 15mL (

72206-001-15)

ACNE TREATMENT CREAM SALICYLIC ACID, 59mL (

72206-001-59)

ACNE TREATMENT CREAM SALICYLIC ACID, 30ML (

72206-001-00)

INGREDIENTS AND APPEARANCE

ACNE TREATMENT 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72206-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
SHEA BUTTER (UNII: K49155WL9Y)
ROSA MOSCHATA OIL (UNII: J99W255AWF)
OLIVE OIL (UNII: 6UYK2W1W1E)
SALIX ALBA BARK (UNII: 205MXS71H7)
MILK THISTLE (UNII: U946SH95EE)
HOPS (UNII: 01G73H6H83)
SQUALENE (UNII: 7QWM220FJH)
ISOCETYL PALMITATE (UNII: 355356620Z)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIMETHICONE (UNII: 92RU3N3Y1O)
TOCOPHEROL (UNII: R0ZB2556P8)
TEA TREE OIL (UNII: VIF565UC2G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
RACEMENTHOL (UNII: YS08XHA860)
HYALURONIC ACID (UNII: S270N0TRQY)
VITIS VINIFERA SEED (UNII: C34U15ICXA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72206-001-15	1 in 1 CARTON	09/01/2017	05/01/2021
1		15 mL in 1 BOX; Type 0: Not a Combination Product
2	NDC: 72206-001-59	1 in 1 CARTON	09/01/2017
2		59 mL in 1 BOX; Type 0: Not a Combination Product
3	NDC: 72206-001-00	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2017	05/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/01/2017	05/01/2021

Labeler - COB Ecommerce Empire LLC (081031434)