BY NATURE DAILY FACE SUNSCREEN BROAD SPECTRUM SPF 30- octinoxate, titanium dioxide, oxybenzone, avobenzone cream

By Nature Daily Face Sunscreen by

Drug Labeling and Warnings

By Nature Daily Face Sunscreen by is a Otc medication manufactured, distributed, or labeled by Lanocorp Pacific Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Octinoxate 7,50%
Titanium dioxide 5,00%
Oxybenzone 4,50%
Avobenzone 2,5%

PURPOSE

Sunscreen

USES

Helps prevent sunburn

WARNINGS

For external use only.
Do not use on broken or damaged skin.

When using this product, keep out of eyes.
Rinse with water to remove.

Stop use and ask a doctor if any rush occurs.

Keep out of reach of children.
If product is swalowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Apply liberally and evenly 15 minutes before sun exposure
Children under 6 months of age: Ask a doctor
Apply to all skin exposed to the sun
Reapply at least every 2 hours
Use a water resistant sunscreen if swimming or sweating
Sun protection measures: Spending time in the sun increases your risk of skin cancer and early skin aging.
To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
 - limit time in the sun, especially from 10am-2pm.
 - wear long-sleeved shirts, pants, hats and sunglasses.

OTHER INFORMATION

Protect the product in this container from excessive heat and direct sun

INACTIVE INGREDIENTS

Aqua (water)
Stearic Acid
Persea Gratissima (Avocado) Oil
Simmondsia Chinensis (Jojoba) Oil
Butyloctyl salicylate
Acetylated Lanolin Alcohol
Leptospermum Scoparium Mel
Actinidia Chinensis (Kiwi) Fruit Extract
Hydrolyzed (Marine) Collagen
Tocopheryl Acetate (Vitamin E)
Carbomer
Cetyl Alcohol
Triethanolamine
Caprylhydroxamic Acid
Phenoxiethanol
Methylpropanediol
Tetrasodium EDTA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BY NATURE DAILY FACE SUNSCREEN   BROAD SPECTRUM SPF 30
octinoxate, titanium dioxide, oxybenzone, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43617-3417
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 g  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	50 g  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	45 g  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	25 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
AVOCADO OIL (UNII: 6VNO72PFC1)
JOJOBA OIL (UNII: 724GKU717M)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
HONEY (UNII: Y9H1V576FH)
KIWI FRUIT (UNII: 71ES77LGJC)
HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW) (UNII: 2WID9OCG7P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
CETYL ALCOHOL (UNII: 936JST6JCN)
TROLAMINE (UNII: 9O3K93S3TK)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43617-3417-3	1 in 1 BOX
1		60 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/01/2014

Labeler - Lanocorp Pacific Ltd (594482114)

Establishment
Name	Address	ID/FEI	Business Operations
Lanocorp Pacific Ltd		594482114	manufacture(43617-3417)