FDA.reportPublic FDA data

Acne Treatment Gel

Manufacturer
Wasatch Product Development, Inc. | Natures Sunshine Products
Effective date
2010-06-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:24:56

Label at a glance#

ProductNatria Acne Treatment
Active ingredientSALICYLIC ACID
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Salicylic Acid            1%

WARNINGS SECTION

Warning: For external use only. Avoid contact with eyes. Rinse with water if eye contact occurs. Discontinue use and contact a doctor if irritation develops and persists.

INDICATIONS & USAGE SECTION

Application: Apply a thin layer evenly over face until completely absorbed. Follow with moisturizer as needed. Use morning and evening.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Butylene Glycol, Antemisia Princeps extract, algae extract, alpha-glucan oligosaccharide, Glycyrrhiza glabra (licorice) root extract, Retinyl Palmitate (Vitamine A), Panthenyl Triacetate (Vitamin B), Tetrahexyldecyl Ascorbate (Vitamin C), Tocopheryl Acetate (Vitamin E), Aloe Barbadensis, Camellia Oleifera (Green tea) leaf extract, Chamomilla recutita (matricaria) flower extract, Ginkgo biloba leaf extract, panax ginseng root extract, ulva lactuca (sea lettuce) extract, Vitis vinifera (grape) seed extract, ergothioneine, sclerotium gum, PEG-8 dimethicone, Phenoxyethanol, Methylparaben, Butylparaben, Ethylparaben, Propylparaben.
image of seconday package label
image of seconday package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Natria

Acne Treatment Gel

30 ml/ 1 fl. oz.

image of primary labelimage of primary label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
417424salicylic acid 1 % Topical CreamPSN3
417424salicylic acid 10 MG/ML Topical CreamSCD3
417424salicylic acid 1 % Topical CreamSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44717-535-022019-10-21C16284748780-1956f9ecf-c354-621f-e053-dbdaa90a74adAcne Treatment Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44717-535-01NatriaAcne Treatment30 mL in 1 TUBECREAM303
44717-535-02NatriaAcne Treatment1 in 1 BOXCREAM13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44717-535NATRIA ACNE TREATMENT (SALICYLIC ACID) CREAM [WASATCH PRODUCT DEVELOPMENT, INC. ]3Legacy NDC, 2 package rows20100630_2ffec18b-5611-4dc1-95d7-aa0084f93f2e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ3
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ3

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44717-53544717-535-01, 44717-535-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML · Source PDF

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
5b0cf83e-5231-4d7b-bd21-312348a7d2012ffec18b-5611-4dc1-95d7-aa0084f93f2e2010-06-30WarningsExact identifier
spl id: 5b0cf83e-5231-4d7b-bd21-312348a7d201
spl set id: 2ffec18b-5611-4dc1-95d7-aa0084f93f2e

Reported adverse events (FAERS/openFDA)#

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