Label: DG BODY TONIC- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 55910-101-08 - Packager: DOLGENCORP INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 3, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- USES
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WARNINGS
FOR EXTERNAL USE ONLY
- FLAMMABLE
- KEEP AWAY FROM FIRE OR HEAT SOURCE
ASK DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE
USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT. THIS MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. iF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS OTHERWISE DIRECTED BY A DOCTOR
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DIRECTIONS
- CLEANSE SKIN THOROUGHLY
- MOISTEN A COTTON BALL WITH PRODUCT AND COVER AFFECTED AREA ONE TO THREE TIMES DAILY
- DUE TO EXCESSIVE DRYING OF THE SKIN, START WITH ONE APPLICATION DAILY, INCREASING TO 2 OR 3 IF NEEDED OR AS DIRECTED BY A PHYSICIAN
- IF PEELING OCCURS, REDUCE USE TO ONCE A DAY OR EVERY OTHER DAY
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- LABEL COPY
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INGREDIENTS AND APPEARANCE
DG BODY TONIC
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) ISOCETETH-20 (UNII: O020065R7Z) SULISOBENZONE (UNII: 1W6L629B4K) FD&C RED NO. 40 (UNII: WZB9127XOA) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-101-08 237 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/02/2015 Labeler - DOLGENCORP INC (068331990) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(55910-101)