TULA Skincare Go Away Acne Spot Treatment

Manufacturer
Tula Life LLC
Effective date
2022-12-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:52:49

Label at a glance#

ProductTULA Skincare Go Away Acne Spot Treatment
Active ingredientBENZOYL PEROXIDE
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

Benzoyl Peroxide 5.0%

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, Dimethyl Isosorbide, Glycerin, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Propanediol, Butylene Glycol, Niacinamide, Lactococcus Ferment Lysate, Lactic Acid, Azelaic Acid, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Capryloyl Salicylic Acid, Aloe Barbadensis Leaf Juice, Vaccinium Angustifolium (Blueberry) Fruit Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Zingiber Officinale (Ginger) Root Extract, Citric Acid, Bisabolol, Morinda Citrifolia Extract, Xanthan Gum, Trisodium Ethylenediamine Disuccinate, Tocopherol, 1,2-Hexanediol, Caprylyl Glycol, Carbomer, Silica, Sodium Citrate, Diethylhexyl Sodium Sulfosuccinate, Dimethicone, Ethylhexylglycerin, Hydroxyacetophenone, Isohexadecane, PEG-40 Stearate, Polyglyceryl-2 Isostearate, Polysorbate 80, Potassium Sorbate, Sodium Benzoate, Sodium Chloride, Sodium Hydroxide, Sorbitan Stearate, Phenoxyethanol

Questions or Comments?

OTC - QUESTIONS SECTION

1-844-545-1236

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

72296-040-1572296-040-15

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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4a7d44fe-774d-404b-aad0-8a90fe78375aProduct name420211025
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
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ad75fcfd-a339-42a1-9c60-43ba2c654cfaProduct name120170810
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2a856070-cbe7-4f85-be0f-09885ff91196Product name120150806
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72296-040-152023-07-28C16284748780-1c7ccaba7-1da3-fd44-e053-dadaa90aa01bDRUG FACTS
72296-040-152021-12-24C16284748780-1c7ccaba7-1da3-fd44-e053-dadaa90aa01bDRUG FACTS
72296-040-152021-07-23C16284748780-1c7ccaba7-1da3-fd44-e053-dadaa90aa01bDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72296-040-15TULA Skincare Go Away Acne Spot Treatment1 in 1 CARTONLIQUID15
72296-040-15TULA Skincare Go Away Acne Spot Treatment15 g in 1 TUBELIQUID155

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72296-040TULA SKINCARE GO AWAY ACNE SPOT TREATMENT LIQUID [TULA LIFE LLC]5Legacy NDC, 2 package rows20230101_60eeddcc-2a25-4f9e-87ba-3b1182397766.zip

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72296-04072296-040-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a52ed291-5333-41fc-9def-3a06490b616d60eeddcc-2a25-4f9e-87ba-3b11823977662022-12-31WarningsExact identifier
spl id: a52ed291-5333-41fc-9def-3a06490b616d
spl set id: 60eeddcc-2a25-4f9e-87ba-3b1182397766

Reported adverse events (FAERS/openFDA)#

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