Label: GLYCOLIC ACID 50 BUFFERED SKIN CHEMICAL PEEL solution
GLYCOLIC ACID 35 BUFFERED SKIN CHEMICAL PEEL solution
GLYCOLIC ACID 70 BUFFERED SKIN CHEMICAL PEEL solution
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NDC Code(s):
84785-0016-1,
84785-0016-2,
84785-0016-3,
84785-0016-4, view more84785-0016-5, 84785-0017-1, 84785-0017-2, 84785-0017-3, 84785-0017-4, 84785-0017-5, 84785-0019-1, 84785-0019-2, 84785-0019-3, 84785-0019-4, 84785-0019-5
- Packager: Gazebo Wellness SKIN LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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DOSAGE & ADMINISTRATION
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.
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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
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INDICATIONS & USAGE
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
- ACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GLYCOLIC ACID 50 BUFFERED SKIN CHEMICAL PEEL
glycolic acid 50 buffered skin chemical peel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84785-0016 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID 0.3 mg in 30 mL SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE 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:84785-0016-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 2 NDC:84785-0016-2 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 3 NDC:84785-0016-3 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 4 NDC:84785-0016-4 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 5 NDC:84785-0016-5 480 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 GLYCOLIC ACID 35 BUFFERED SKIN CHEMICAL PEEL
glycolic acid 35 buffered skin chemical peel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84785-0019 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID 0.3 mg in 30 mL SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE 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:84785-0019-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 2 NDC:84785-0019-2 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 3 NDC:84785-0019-3 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 4 NDC:84785-0019-4 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 5 NDC:84785-0019-5 480 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 GLYCOLIC ACID 70 BUFFERED SKIN CHEMICAL PEEL
glycolic acid 70 buffered skin chemical peel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84785-0017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE 0.3 mg in 30 mL GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC 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:84785-0017-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 2 NDC:84785-0017-2 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 3 NDC:84785-0017-3 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 4 NDC:84785-0017-4 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 5 NDC:84785-0017-5 480 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(84785-0019, 84785-0017, 84785-0016)
