- Active Ingredients
- Purpose
- Uses
-
Warnings
For external use only
Using other topical medications at the same time or
immediately following use of this product may increase
dryness or irritation of the skin. If this occurs, only one
medication should be used unless directed by a doctor.When using this product
• avoid contact with the eyes
• if contact occurs, rinse thoroughly with water - Keep out of reach of children
-
Directions
• clean the skin thoroughly before applying this product
• cover the entire affected area with a thin layer one to three
times daily
• 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 -
Inactive ingredients
Water/Aqua/Eau, Sodium Polyacrylate, Sodium PCA, Glycerin, Polyacrylate Crosspolymer-6, Azelaic Acid, Lactococcus Ferment Lysate, Zinc PCA, Epilobium Angustifolium Flower/Leaf/Stem Extract, Niacinamide, Bisabolol, Allantoin, Sodium Hyaluronate, Lactic Acid, Sodium Benzoate, Sodium Chloride, Sodium Metabisulfite, Ehtylhexylglyceirn, Phenoxyethanol
- Questions or Comments?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
TULA ACNE CLEARING AND TONE CORRECTING GEL
tula acne clearing and tone correcting gel liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72296-010 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 g Inactive Ingredients Ingredient Name Strength NIACINAMIDE (UNII: 25X51I8RD4) .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z) ALLANTOIN (UNII: 344S277G0Z) LACTIC ACID (UNII: 33X04XA5AT) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM METABISULFITE (UNII: 4VON5FNS3C) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) SODIUM (UNII: 9NEZ333N27) GLYCERIN (UNII: PDC6A3C0OX) AZELAIC ACID (UNII: F2VW3D43YT) LACTOCOCCUS LACTIS (UNII: F1A0PSN10V) ZINC (UNII: J41CSQ7QDS) EPILOBIUM ANGUSTIFOLIUM LEAF (UNII: 7NV86426N2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72296-010-30 1 in 1 CARTON 07/24/2018 1 30 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 07/24/2018 Labeler - Tula Life LLC (080051358)