FIRST AID BEAUTY ANTI-DANDRUFF SCALP SERUM- salicylic acid liquid 
The Procter & Gamble Manufacturing Company

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.

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First Aid Beauty Anti-Dandruff Scalp Serum

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Anti-dandruff

Uses

helps eliminate and reduces recurrence of the symptoms of dandruff.

Warnings

For external use only.

When using this product

  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

  • condition worsens or does not improve after regular use of this product as directed.

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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)?

888-FAB-3063

MADE IN USE.

DISTR. BY: FIRST AID BEAUTY ® LTD

NEWTON, MA 02458

PRINCIPAL DISPLAY PANEL - carton label

First Aid Beauty

Anti-Dandruff

Scalp Serum

2% Salicylic Acid

Safe for sensitive skin

Dermatologist tested

No Artificial Fragrance

88.7 mL (3 FL OZ)

FAB

FIRST AID BEAUTY ANTI-DANDRUFF SCALP SERUM 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-592
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-592-881 in 1 CARTON07/30/2021
188.7 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H07/30/2021
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 2/2022
Document Id: d6fad997-2788-7aec-e053-2995a90ac086
Set id: d22ab93f-c4ff-07a4-e053-2a95a90a0a3f
Version: 2
Effective Time: 20220201
 
The Procter & Gamble Manufacturing Company