TULA ACNE CLEARING AND TONE CORRECTING GEL liquid

TULA acne clearing and tone correcting gel by

Drug Labeling and Warnings

TULA acne clearing and tone correcting gel by is a Otc medication manufactured, distributed, or labeled by Tula Life LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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INGREDIENTS AND APPEARANCE

TULA ACNE CLEARING AND TONE CORRECTING GEL 
tula acne clearing and tone correcting gel liquid

Product 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)