By Nature Daily Face Sunscreen description, usages, side effects, indications, overdosage, supplying and lots more!

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By Nature Daily Face Sunscreen

Lanocorp Pacific Ltd

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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


By Nature Daily Face Sunscreen



By Nature Daily Face Sunscreen

By Nature Daily Face Sunscreen

OCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE, AVOBENZONE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43617-3417
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 g
titanium dioxide 50 g
OXYBENZONE OXYBENZONE 45 g
AVOBENZONE AVOBENZONE 25 g

Inactive Ingredients

Ingredient Name Strength
water
STEARIC ACID
AVOCADO OIL
Jojoba Oil
BUTYLOCTYL SALICYLATE
ACETYLATED LANOLIN ALCOHOLS
HONEY
KIWI FRUIT
HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW)
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
CETYL ALCOHOL
TROLAMINE
CAPRYLHYDROXAMIC ACID
PHENOXYETHANOL
methylpropanediol
EDETATE SODIUM

Packaging

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

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2014-02-01


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