NATRIA NOURISHING DAILY DEFENSE- ethylhexyl 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

Octinoxate   7.5%

Zinc Oxide   3%

Warnings: For external use only. Avoid contact with eyes. Rinse with water if eye contact occurs. Discontinue use and consult a doctor if rash or irritation develops and persists. Keep out of reach of children.

Application: with fingertips, smooth gently and evenly over face and neck

Inactive Ingredients: Water (Aqua), Ethylhexyl Methoxycinnamate, Pentylene Glycol, Ethylhexyl Isononanoate, Octyldodecyl Neopentanoate, Sucrose Cocoate, Cetearyl Alcohol, Glycerin, Zinc Oxide, Caprylic/Capric Triglyceride, Zea mays (corn) oil, glycine soja (soybean) seed extract, glycine soja (soybean) lipids, polyglyceryl-3 distearate, steareth-20, phenoxyethanol, chloraphenesin, glycerin, methylparaben, benzoic acid, squalane, algae extracts, artemisia princeps leaf extract, behenyl alcohol, phytosteryl isostearate, magnesium aluminum silicate, potassium cetyl phosphate, Theobroma cacao (Cocoa) seed butter, xanthan gum, dimethicone copolyol, tocopheryl acetate (vitamin E), prunus amygdalus (sweet almond) oil, prunus armensca (apricot) kernel oil, lecithin, plankton extract, fragrance (essential oils), disodium EDTA, tetrahexyldecyl ascorbate (vitamin C), panthenyl triacetate (vitamin B), panax ginseng root extract, chamomilla recutita (marticaria) flower extract, ulva lactuca (sea lettucs) extract, ginkgo biloba leaf extract, sodium PCA, retinyl palmitate (vitamin A), ergothioneine, aloe barbadensis, vitis vinifera (grape) seed extract, camellia oleifera (green tea) leaf extract, dimethicone, citric acid.

PRINCIPAL DISPLAY PANEL

Natria

Nourishing Daily Defense Lotion SPF 15

75 ml/ 2.5 fl.oz.

INGREDIENTS AND APPEARANCE

NATRIA  NOURISHING DAILY DEFENSE
ethylhexyl methoxycinnamate, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44717-533
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44717-533-02	1 in 1 BOX
1	NDC: 44717-533-01	75 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	01/01/2010

Labeler - Wasatch Product Development (962452533)

Registrant - Nature's Sunshine (081832388)

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