Label: DERMAREST PSORIASIS MEDICATED- salicylic acid liquid
- NDC Code(s): 63736-302-24
- Packager: Insight Pharmaceuticals LLC
- 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 January 10, 2020
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Inactive ingredients
Purified water, ammonium lauryl sulfate, sodium laureth sulfate, sodium citrate, cocamidopropyl betaine, lauryl glucoside, PEG-150 pentaerythrityl tetrastearate, coco-glucoside, glyceryl oleate, aleurites moluccana seed oil, zinc PCA, panthenol, rheum palmatum extract, carthamus tinctorius (safflower) flower extract, camellia sinensis leaf extract, edetate disodium
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INGREDIENTS AND APPEARANCE
DERMAREST PSORIASIS MEDICATED
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-302 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM CITRATE (UNII: 1Q73Q2JULR) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) KUKUI NUT OIL (UNII: TP11QR7B8R) ZINC PIDOLATE (UNII: C32PQ86DH4) PANTHENOL (UNII: WV9CM0O67Z) RHEUM PALMATUM WHOLE (UNII: 75P857ARCY) SAFFLOWER (UNII: 4VBL71TY4Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) EDETATE DISODIUM (UNII: 7FLD91C86K) Product Characteristics Color WHITE (Clear) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63736-302-24 1 in 1 CARTON 07/23/2010 1 236 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part358H 07/23/2010 Labeler - Insight Pharmaceuticals LLC (055665422)