TULA breakout star oil-free acne moisturizer

Manufacturer
Tula Life LLC
Effective date
2024-03-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:10:12

Label at a glance#

ProductTULA breakout star oil-free acne moisturizer
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

• treats acne • Helps prevent the development or new acne blemishes

Dosage and administration

• 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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2.0%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

• treats acne

• Helps prevent the development or new acne blemishes

Warnings

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Propanediol, Dimethicone, Glycerin, Dimethyl Isosorbide, Lactococcus Ferment Lysate, Polysorbate 20, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Niacinamide, Aloe Barbadensis Leaf Juice, Azelaic Acid, Bisabolol, Cetearyl Olivate, Cirusllus Lanatus (Watermelon) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Citrus Aurantium Dulcis (Orange) Peel Extract, Epilobium
Angustifolium Flower/Leaf/Stem Extract, Lactic Acid, Lens Esculenta (Lentil) Fruit Extract, Ocimum Sanctum Leaf Extract, Ozonized Oryza Sativa (Rice) Callus Culture Extract, Phenoxyethanol, Polyacrylate Crosspolymer-6, Saccharide Isomerate, Sodium Chloride, Sodium Lactate, Sodium PCA, Sorbitan Isostearate, Sorbitan Olivate, Trisodium Ethylenediamine Disuccinate, Ethylhexylglycerin, Xanthan Gum

Questions or Comments?

OTC - QUESTIONS SECTION

1-844-545-1236

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

72296-020-50v3 72296-020-50 Image72296-020-50 Image

72296-020-15v3

72296-020-15 Image72296-020-15 Image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
6c6fc281-9445-2e9e-1c29-a09ddbc4299cProduct name220200213
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
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597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72296-02072296-020-50, 72296-020-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
28a7451b-8cf0-efc4-e063-6294a90a42673951ea9f-26f2-4508-b2ea-a77ec9e29ddf2024-12-06WarningsExact identifier
spl set id: 3951ea9f-26f2-4508-b2ea-a77ec9e29ddf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.