Label: BASIC ESSENTIALS ASTRINGENT- salicylic acid solution
- NDC Code(s): 73597-021-08
- Packager: Mission Series Inc. dpa Prestige Beauty Care
- 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 May 1, 2023
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- Purpose
- Active Ingredient
- Indications & Usage
- Warnings
- When using this product
- Ask a doctor
- Keep out of reach of children
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Directions
Directions: • Wash face as you normally would and pat dry with a clean towel. • Apply a small amount to cotton ball or pad and apply using a dabbing motion. • Take care to avoid rubbing in eyes. • Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy. • Apply a light moisturizer after using astringent. • If bothersome drying or peeling occurs, reduce application.
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Inactive Ingredients
Inactive ingredients Water, Ethyl Alcohol, Propylene Glycol, Glycerin, PEG 400, PEG 40 Hydrogenated Castor Oil, Cocamidopropyl Betaine, Hydroxythylcellulose, Fragrance, Sodium Citrate, Phenoxyethanol, Disodium EDTA, Algae Extract, Aloe Barbadensis Leaf Extract, Benzophenone 4, FD & C Blue 1, FD & C Yellow 5
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INGREDIENTS AND APPEARANCE
BASIC ESSENTIALS ASTRINGENT
salicylic acid solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73597-021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.05 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) SODIUM CITRATE (UNII: 1Q73Q2JULR) WATER (UNII: 059QF0KO0R) SULISOBENZONE (UNII: 1W6L629B4K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PHENOXYETHANOL (UNII: HIE492ZZ3T) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) BENZOPHENONE (UNII: 701M4TTV9O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73597-021-08 236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 05/01/2023 Labeler - Mission Series Inc. dpa Prestige Beauty Care (117190866)