Label: LACTIC ACID 35 SKIN CHEMICAL PEEL solution
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NDC Code(s):
84785-0021-1,
84785-0021-2,
84785-0021-3,
84785-0021-4, view more84785-0021-5, 84785-0021-6
- Packager: Gazebo Wellness SKIN LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 16, 2024
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- Official Label (Printer Friendly)
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DOSAGE & ADMINISTRATION
Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and use sunscreen. For external use only.
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WARNINGS
DIRECTIONS: Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and use sunscreen. For external use only.
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
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INDICATIONS & USAGE
DIRECTIONS: Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and use sunscreen. For external use only.
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LACTIC ACID 35 SKIN CHEMICAL PEEL
lactic acid 35 skin chemical peel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84785-0021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT) LACTIC ACID 0.3 mg in 30 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84785-0021-1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 2 NDC:84785-0021-2 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 3 NDC:84785-0021-3 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 4 NDC:84785-0021-4 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 5 NDC:84785-0021-5 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 6 NDC:84785-0021-6 480 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 10/01/2024 Labeler - Gazebo Wellness SKIN LLC (119609953) Registrant - Gazebo Wellness SKIN LLC (119609953) Establishment Name Address ID/FEI Business Operations Gazebo Wellness SKIN LLC 119609953 manufacture(84785-0021)