FDA.reportPublic FDA data

Natria Brightening Lotion SPF 15

Manufacturer
Wasatch Product Development | Nature's Sunshine
Effective date
2011-03-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:27:28

Label at a glance#

ProductNatria Brightening SPF 15
Active ingredientOCTINOXATE, ZINC OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Ethylhexyl Methoxycinnamate 7.5%

Zinc Oxide 4%

OTC - PURPOSE SECTION

provides instant hydration and long- lasting defense against UV rays to keep skin clear from discoloration

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

 For external use only.

WARNINGS SECTION

Avoid contact with eyes. Rinse with water if eye contact occurs. Discontinue use and contact a doctor if rash or irritation develops and persists.

DOSAGE & ADMINISTRATION SECTION

with fingertips, smooth gently and evenly over face and neck .

INACTIVE INGREDIENT SECTION

Ingredients: Water (Aqua), Cyclopentasiloxane, Cetearyl Glucoside, Isopentyldiol, C12-15 Alkyl Benzoate, Dimethicone, Glycyrrhiza Glabra (Licorice) Root Extract, Morus Alba (Mulberry) Root Extract, Plankton Extract, Farnesyl Acetate, Farnesol, Glycine Soja (Soybean) Lipids, Retinyl Palmitate (Vitamin 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, Fragrance (Essential Oils), Squalane, Zea Mays (Corn) Oil, Algae Extract, Artemisia Princeps Leaf Extract, Sodium PCA, Ergothioneine, Caprylic/Capric Triglyceride, Behenyl Alcohol, Magnesium Aluminu Silicate, Butylene Glycol, Lecithin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polysorbate 60, Xanthan Gum, Disodium EDTA, Sodium Hydroxide, Glycerin, Phenoxyethanol, Chlorphenesin, Methylparaben, Benzoic Acid.


image of back labelimage of back label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Natria

Brightening Lotion SPF 15

Nature's Sunshine

50 ml 1.7 fl oz

image of front label
image of front label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44717-538-022019-10-29C16284748780-1960f7f55-db08-8e05-e053-dbdaa90a074aNatria Brightening Lotion SPF 15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z2
ALKYL (C12-15) BENZOATEINACTIVE INGREDIENTA9EJ3J61HQ2
CETEARYL GLUCOSIDEINACTIVE INGREDIENT09FUA47KNA2
CYCLOMETHICONE 5INACTIVE INGREDIENT0THT5PCI0R2
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O2
GLYCYRRHIZA GLABRAINACTIVE INGREDIENT2788Z9758H2
ISOPENTYLDIOLINACTIVE INGREDIENT19NOL5474Q2
SODIUM PYRROLIDONE CARBOXYLATEINACTIVE INGREDIENT469OTG57A22
SQUALENEINACTIVE INGREDIENT7QWM220FJH2
TETRAHEXYLDECYL ASCORBATEINACTIVE INGREDIENT9LBV3F07AZ2

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44717-53844717-538-01, 44717-538-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
ZINC OXIDESOI2LOH54ZACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
ISOPENTYLDIOL19NOL5474QIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
SQUALENE7QWM220FJHIACT
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL / TOPICAL2.5 %w/wExact identifier — unii candidate
3 equally ranked IID candidates
SODIUM PYRROLIDONE CARBOXYLATESODIUM PYRROLIDONE CARBOXYLATE469OTG57A2LOTION / TOPICAL42 mgExact identifier — unii candidate
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RCREAM, AUGMENTED / TOPICAL260 mgExact identifier — unii candidate
3 equally ranked IID candidates
CYCLOMETHICONE 5CYCLOMETHICONE 50THT5PCI0RAEROSOL, FOAM / TOPICAL144 mgExact identifier — unii candidate
3 equally ranked IID candidates

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
9412749c-b788-4b7f-8b54-7503da58fb93390d2793-6ee4-44a4-82ae-708bfd039ead2011-03-11WarningsExact identifier
spl id: 9412749c-b788-4b7f-8b54-7503da58fb93
spl set id: 390d2793-6ee4-44a4-82ae-708bfd039ead

Reported adverse events (FAERS/openFDA)#

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