Label: SALICYLIC 10 SKIN PEEL solution
-
NDC Code(s):
84785-0012-1,
84785-0012-2,
84785-0012-3,
84785-0012-4, view more84785-0012-5, 84785-0012-6
- 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)
-
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. -
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
-
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
-
INGREDIENTS AND APPEARANCE
SALICYLIC 10 SKIN PEEL
salicylic 10 skin peel solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84785-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.3 mg in 30 mL Inactive Ingredients Ingredient Name Strength HEXYLENE GLYCOL (UNII: KEH0A3F75J) BENZALDEHYDE PROPYLENE GLYCOL ACETAL (UNII: ELQ3FTL5B1) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84785-0012-1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 2 NDC:84785-0012-2 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 3 NDC:84785-0012-3 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 4 NDC:84785-0012-4 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 5 NDC:84785-0012-5 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2024 6 NDC:84785-0012-6 480 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(84785-0012)
