Label: FIRST AID BEAUTY ANTI-DANDRUFF SCALP SERUM- salicylic acid liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 69423-592-88 - Packager: The Procter & Gamble Manufacturing Company
- 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 1, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive ingredients
water, aloe barbadensis leaf juice, polysorbate 20, glycerin, mentlloxypropanediol, phenoxyethanol, sodium hydroxide, propanediol, sodium pca, citric acid, sodium citrate, caprylyl/capryl glucoside, chrysanthemum parthenium (feverfew) extract, hydroxyethylcellulose, calendula officinalis flower extract, camellia sinensis leaf extract, DL panthenol, glycyrrhiza glabra (licorice) root extract, lavandula hybrida (lavandin) oil, rosmarinus officinalis (rosemary) leaf oil, colloidal oatmeal, mentha arvensis leaf oil, sodium hyaluronate, potassium sorbate, sodium benzoate, linalool, vanillyl butyl ether, decyl alcohol, caprylyl alcohol, charcoal powder, disodium phosphate, polysorbate 60, tetrasodium EDTA, sodium phosphate, glucose
- Questions (or comments)?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - carton label
-
INGREDIENTS AND APPEARANCE
FIRST AID BEAUTY ANTI-DANDRUFF SCALP SERUM
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-592 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PROPANEDIOL (UNII: 5965N8W85T) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM PHOSPHATE (UNII: SE337SVY37) 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM BENZOATE (UNII: OJ245FE5EU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LAVANDIN OIL (UNII: 9RES347CKG) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) POLYSORBATE 60 (UNII: CAL22UVI4M) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CAPRYLIC ALCOHOL (UNII: NV1779205D) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K) OATMEAL (UNII: 8PI54V663Y) DECYL ALCOHOL (UNII: 89V4LX791F) WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) PHENOXYETHANOL (UNII: HIE492ZZ3T) PANTHENOL (UNII: WV9CM0O67Z) ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) GLYCERIN (UNII: PDC6A3C0OX) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) ALOE VERA LEAF (UNII: ZY81Z83H0X) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ROSEMARY OIL (UNII: 8LGU7VM393) SODIUM HYDROXIDE (UNII: 55X04QC32I) LINALOOL, (+/-)- (UNII: D81QY6I88E) SODIUM CITRATE (UNII: 1Q73Q2JULR) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-592-88 1 in 1 CARTON 07/30/2021 1 88.7 mL in 1 BOTTLE, PLASTIC; 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 07/30/2021 Labeler - The Procter & Gamble Manufacturing Company (004238200)