Label: SKINLYCIOUS GLOW EXFOLIANT- salicylic acid liquid
- NDC Code(s): 81574-001-01, 81574-001-02, 81574-001-03
- Packager: Skinlycious Pte Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 8, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For External Use Only
Do not use if you
• are pregnant
• are a child under 3 years of age
• are allergic to salicylates
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 unnecessary sun exposure and use a sunscreen.
• Avoid contact with the eyes, lips and mouth.
• First time users may experience tingling sensation and visible peeling. After frequent usage, tingling and peeling will likely reduce.
Stop use and ask a doctor if
• Irritation becomes severe - Keep out of reach of children
- Questions or Comments
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Direction
• Cleanse the skin thoroughly before applying this product
• For treatment of acne, wet cotton bud or pad with solution and cover the entire affected area with a thin layer one to three times daily. Suitable for both facial and body acne.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
• If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
• Complement this with other Skinlycious products to reduce the likelihood of skin dryness.
• For full face exfoliant, wet cotton pad with a solution and apply a thin layer in the evening only over the entire face. No need to rinse off. Once skin condition improves, reduce frequency to no more than 3-5 times a week in the evening only. - Inactive Ingredients
- Other information
- Product label
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INGREDIENTS AND APPEARANCE
SKINLYCIOUS GLOW EXFOLIANT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81574-001 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 WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) MANDELIC ACID (UNII: NH496X0UJX) GLYCERIN (UNII: PDC6A3C0OX) PURSLANE (UNII: M6S840WXG5) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81574-001-01 28 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/01/2021 2 NDC:81574-001-02 5 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/01/2021 3 NDC:81574-001-03 8 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/01/2021 Labeler - Skinlycious Pte Ltd (595402258) Establishment Name Address ID/FEI Business Operations CHAKS COSMETIC DESIGN & SERVICES PTE LTD 595557596 manufacture(81574-001)