TULA ACNE CLEARING AND TONE CORRECTING GEL- tula acne clearing and tone correcting gel liquid 
Tula Life LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DRUG FACTS

Active Ingredients

Salicylic Acid 2.0%

Purpose

Acne Treatment

Uses

• treats acne

• Helps prevent the development or new acne blemishes

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

Keep out of reach of children. If swallowed, get medical help
or contact a Poison Control Center right away.

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?

1-844-545-1236

Principal Display Panel

30 ml Package

72296-010-3015 mL Sample

72296-010-15

TULA ACNE CLEARING AND TONE CORRECTING GEL 
tula acne clearing and tone correcting gel liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72296-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
GLYCERIN (UNII: PDC6A3C0OX)  
AZELAIC ACID (UNII: F2VW3D43YT)  
LACTOCOCCUS LACTIS (UNII: F1A0PSN10V)  
ZINC (UNII: J41CSQ7QDS)  
EPILOBIUM ANGUSTIFOLIUM LEAF (UNII: 7NV86426N2)  
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)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72296-010-301 in 1 CARTON12/26/2022
130 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:72296-010-151 in 1 CARTON12/26/2022
215 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D12/26/2022
Labeler - Tula Life LLC (080051358)

Revised: 12/2022
Document Id: d8df491f-d0ec-43f8-b401-b7e051f5005c
Set id: fe742404-9a2f-433c-bcf8-904231c16400
Version: 3
Effective Time: 20221226
 
Tula Life LLC