UNAGEL- salicylic acid cream 
Advanced Skin Technology, LLC

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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Unagel

Drug Facts

Active Ingredient

Salicylic Acid 2 percent

Purpose

Acne Medication

Uses

for the treatment of acne

Warnings

For External Use Only

When using this product with other topical medications, increased dryness or irritation of the skin may occur. If this occurs, only one medication should be used unless directed by a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Directions

  • cleanse thoroughly before applying medication.
  • cover affected area with thin layer one to three times daily.
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • recommended for daily use.

Inactive ingredients

aqua, disodium phosphate, propylene glycol, butylene glycol, PEG-12 dimethicone, carbomer, triethanolamine, phragmites, kharka extract, poria cocos extract, camellia oleifera (green tea) leaf extract, xanthan gum, disodium EDTA, alkyl acrylate, methacrylate copolymer, propyl alcohol, phenoxyethanol, vitis vinifera (grape) seed oil, methylparaben, butylparaben, ethylparaben, propyl paraben, menthol

Questions

1-866-642-7546

www.AdvancedSkinTech.com

BENEFITS

Prevents acne by promoting gentle exfoliation which can unclog pores.
Penetrates the pore to treat acne blemishes.
Helps reduce the appearance of irritated redness.
Reduces the number and severity of acne blemishes.
Helps prevent the formation of new acne and allows the skin to heal itself.
Light, non-greasy gel formulation feels cool and gentle to the skin.
Non-pore clogging, fragrance free formula.
Ideal formula for sensitive skin.

Best results can be achieved when used in conjunction with a topical retinoid like Green Cream - high potency retinol



CARE AND CAUTION

Test a small patch of skin and wait 24 hours before you continue use of this product.
Wear a broad-spectrum sunscreen while using this product.
Avoid contact with the eyes. If product gets in the eye, rinse thoroughly with water.
Suspend use if skin becomes irritates. Seek medical help if reaction is severe.
For external use only; do not ingest.
Keep out of reach of children.
Do not use if allergic to aspirin.

Disclaimer: This product is an active product that should be used with caution and care. Please read all instructions and contact us if you have any questions or concerns. Advanced Skin Technology, LLC does not make any warranties; whether expressed or implied with respect to the use of this product as it relates to fitness for a particular purpose, or for any other matter. The buyer's sole remedy for any claim against the manufacturer or distributor shall be limited to the replacement of the product.

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UNAGEL 
salicylic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52205-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PHRAGMITES KARKA WHOLE (UNII: 10086A360Y)  
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
PROPYL ALCOHOL (UNII: 96F264O9SV)  
WATER (UNII: 059QF0KO0R)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
TROLAMINE (UNII: 9O3K93S3TK)  
FU LING (UNII: XH37TWY5O4)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GRAPE SEED OIL (UNII: 930MLC8XGG)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
ETHYLPARABEN (UNII: 14255EXE39)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
MENTHOL (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52205-001-0029 g in 1 BOTTLE; Type 0: Not a Combination Product09/04/201205/25/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D09/04/201205/25/2022
Labeler - Advanced Skin Technology, LLC (130977940)
Establishment
NameAddressID/FEIBusiness Operations
Advanced Skin Technology, LLC130977940manufacture(52205-001)

Revised: 5/2022
 
Advanced Skin Technology, LLC