NATRIA BRIGHTENING SPF 15- ethylhexl methoxycinnamate, zinc oxide cream

Natria by

Drug Labeling and Warnings

Natria by is a Otc medication manufactured, distributed, or labeled by Wasatch Product Development, Nature's Sunshine. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Ethylhexyl Methoxycinnamate 7.5%

Zinc Oxide 4%

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

Keep out of reach of children.

 For external use only.

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

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

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.

PRINCIPAL DISPLAY PANEL

Natria

Brightening Lotion SPF 15

Nature's Sunshine

50 ml 1.7 fl oz

INGREDIENTS AND APPEARANCE

NATRIA  BRIGHTENING SPF 15
ethylhexl methoxycinnamate, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44717-538
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 mL  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	2.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
ISOPENTYLDIOL (UNII: 19NOL5474Q)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
SQUALENE (UNII: 7QWM220FJH)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44717-538-02	1 in 1 BOX
1	NDC: 44717-538-01	50 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/19/2010

Labeler - Wasatch Product Development (962452533)

Registrant - Nature's Sunshine (081832388)

Establishment
Name	Address	ID/FEI	Business Operations
Wasatch Product Development		962452533	manufacture