FIRST AID BEAUTY FAB ACNE SPOT TREATMENT- salicylic acid gel 
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 FAB Acne Spot Treatment Gel

Drug Facts

Active ingredients

Salicylic Acid 2%

Purpose

Acne Treatment

Uses

Warnings

For external use only.

When using this product

  • Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if skin irritation occurs/gets worse.

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

Directions

Water, butylene glycol, hydroxyethylcellulose,glycerin, phenoxyethanol, sodium hydroxide, glycolic acid, urea, aloe barbadensis leaf juice, bisabolol, colloidal oatmeal, maltodextrin, carica papaya (papaya) fruit extract, potassium sorbate, sodium benzoate, camellia sinensis leaf extract, chrysanthemum parthenium (feverfew) extract, glycyrrhiza glabra (licorice) root extract, salix nigra (willow) bark extract, disodium phosphate, polysorbate 60, leuconostoc/radish root ferment filtrate, sodium phosphate, citric acid

Questions:

888-FAB-3063

MADE IN USA

FIRST AID BEAUTY LTD

NEWTON, MA 02458

WWW.FIRSTAIDBEAUTY.COM

PRINCIPAL DISPLAY PANEL - 22 mL carton

FIrst Aid Beauty ®

FAB

ACNE SPOT

TREATMENT GEL

2% Salicylic Acid

Safe for sensitive skin

22 mL (0.75 FL OZ)

FAB

FIRST AID BEAUTY FAB ACNE SPOT TREATMENT 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-724
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
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
OATMEAL (UNII: 8PI54V663Y)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
UREA (UNII: 8W8T17847W)  
LEVOMENOL (UNII: 24WE03BX2T)  
TANACETUM PARTHENIUM FLOWER (UNII: 7TVV9D7I89)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
PAPAYA (UNII: KU94FIY6JB)  
SALIX NIGRA BARK (UNII: QU52J3A5B3)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-724-221 in 1 CARTON08/01/2023
122 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00608/01/2023
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 7/2023
Document Id: 018e1bfe-e100-46d3-e063-6394a90af69b
Set id: 018e4aad-2e37-d7e9-e063-6394a90a9de2
Version: 1
Effective Time: 20230728
 
The Procter & Gamble Manufacturing Company