DR DENNIS GROSS ALL-OVER BLEMISH- salicylic acid gel

dr dennis gross All-Over Blemish by

Drug Labeling and Warnings

dr dennis gross All-Over Blemish by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active ingredient

Salicylic Acid 2.0%

Purpose

Acne Treatment

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.

Uses

• for the treatment and management of acne
• penetrates pores to eliminate most acne blemishes and blackheads
• helps prevent development of new acne blemishes and blackheads
  

Warnings

For external use only.

When using this product

• using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
  

Directions

• cleanse skin thoroughly before applying
• cover the entire affected area AM or PM
• if bothersome dryness or peeling occurs, reduce application to every other day.
  

Inactive ingredients

Cyclopentasiloxane, Dimethicone Crosspolymer, Dimethicone/Vinyltrimethylsiloxysilicate Crosspolymer, Squalane, Dimethicone/Vinyl Dimethicone Crosspolymer, Ubiquinone, Disodium EDTA, Bisabolol, Menthol, Phenoxyethanol, Farnesol

dr.dennis gross All-Over Blemish Product Label

dr.dennisgross™
SKINCARE

All-Over
Blemish
Solution

Salicylic Acid
Acne Treatment Gel

Pore Minimizer for Sensitive Skin

DERMATOLOGIST APPROVED HYPOALLERGENIC

1.7 fl oz/50mL e

Eliminates and prevents blackheads
Controls oil and shine
Non-drying for sensitive, acne-prone skin

PARABEN FREE

Dr. Dennis Gross Skincare™  LLC.,
Dist. NY, NY 10022
dgskincare.com
MD031521

VEGAN

INGREDIENTS AND APPEARANCE

DR DENNIS GROSS ALL-OVER BLEMISH  
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-124
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE PEG-7 PHOSPHATE (UNII: WTP86Y84TV)
CYCLOMETHICONE 4 (UNII: CZ227117JE)
SQUALANE (UNII: GW89575KF9)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
UBIDECARENONE (UNII: EJ27X76M46)
EDETATE DISODIUM (UNII: 7FLD91C86K)
LEVOMENOL (UNII: 24WE03BX2T)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FARNESOL (UNII: EB41QIU6JL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-124-50	50 mL in 1 TUBE; Type 0: Not a Combination Product	11/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/01/2009

Labeler - Bentley Laboratories, LLC (068351753)

Registrant - Bentley Laboratories, LLC (068351753)

Establishment
Name	Address	ID/FEI	Business Operations
Bentley Laboratories, LLC		068351753	manufacture(54111-124)