Label: SALICYLIC ACID- astringent liquid
- NDC Code(s): 55301-875-34
- Packager: Your Military Exchanges
- 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 February 25, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer and rinse thoroughly 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 daily application to once a day or every other day
- Inactive ingredients
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SPL UNCLASSIFIED SECTION
Gently cleans and refreshes by removing oil and dirt
Delicate formula that helps treat and prevent pimples
*This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Clean & Clear Sensitive Skin Deep Cleaning Astringent.
SATISFACTION GUARANTEED
OR YOUR MONEY BACK
Manufactured For Your Military Exchanges
By: Vi-Jon, 8515 Page Avenue
St. Louis, MO 63114
DSP-TN-15000 DSP-MO-34 SDS-TN-15012
875.002/875AE
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
astringent liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55301-875 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 ALCOHOL (UNII: 3K9958V90M) LAMINARIA DIGITATA (UNII: 15E7C67EE8) ALOE VERA LEAF (UNII: ZY81Z83H0X) SULISOBENZONE (UNII: 1W6L629B4K) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A) GLYCERIN (UNII: PDC6A3C0OX) ISOCETETH-20 (UNII: O020065R7Z) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CITRATE (UNII: 1Q73Q2JULR) water (UNII: 059QF0KO0R) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55301-875-34 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/05/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/05/2009 Labeler - Your Military Exchanges (001695568)