DG DEEP CLEANING ASTRINGENT SENSITIVE SKIN- salicylic acid liquid

DG Deep Cleaning Astringent Sensitive Skin by

Drug Labeling and Warnings

DG Deep Cleaning Astringent Sensitive Skin by is a Otc medication manufactured, distributed, or labeled by BELVEDERE INTERNATIONAL INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

DRUG FACTS

Active Ingredient

Salicylic acid 0.50%

USE for treatment of acne

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

INDICATIONS & USAGE

USE FOR TREATMENT OF ACNE

WARNINGS

FOR EXTERNAL USE ONLY, Flammable, keep awat from open fire or flame, Using other topical acne medication at the same time or immediately following the use fo this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Rinse right away with water if it gets in eyes.

DOSAGE & ADMINISTRATION

• CLEANSE SKIN THOROUGHLY BEFORE APPLYING MEDICATION
• MOISTEN A COTTON BALL AND COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER 1 TO 3 TIMES DAILY
• BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH 1 APPLICATION DAILY. THEN GRADUALLY INCREASE TO 2 OR 3 TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCOR. IF BOTHERSOME DRYING OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.

INACTIVE INGREDIENT

WATER, Alcohol, Glycerin, Isoceteth-20, Sodium Citrate, Fragrance, Propylene Glycol, Benzophenone-4, Algae extract, Aloe barbadensis leaf extract, triethanolamine, denatonium benzoate, blue 1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DG DEEP CLEANING ASTRINGENT SENSITIVE SKIN 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60742-002
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)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
ISOCETETH-20 (UNII: O020065R7Z)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BENZOPHENONE (UNII: 701M4TTV9O)
ALOE (UNII: V5VD430YW9)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60742-002-01	240 g in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333D	01/31/2013

Labeler - BELVEDERE INTERNATIONAL INC. (247836356)

Registrant - BELVEDERE INTERNATIONAL INC. (247836356)

Establishment
Name	Address	ID/FEI	Business Operations
BELVEDERE INTERNATIONAL INC.		247836356	manufacture(60742-002)