ATOMY SUN description, usages, side effects, indications, overdosage, supplying and lots more!

ATOMY SUN

ATOMY CO., LTD.
ATOMY CO., LTD.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts



FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients: OCTINOXATE 7.5%, OCTISALATE 5%, ZINC OXIDE 4.9%, TITANIUM DIOXIDE 2.49%

Inactive ingredients:
WATER, CYCLOMETHICONE 5, GLYCERIN, DIPROPYLENE GLYCOL, PEG-10 DIMETHICONE, CYCLOMETHICONE, TALC, DISTEARDIMONIUM HECTORITE, GREEN TEA LEAF, THYME OIL, MELISSA OFFICINALIS, ALTHAEA OFFICINALIS LEAF, PERILLA FRUTESCENS LEAF, CENTELLA ASIATICA, BORAGE, JASMINUM OFFICINALE FLOWER, MAGNESIUM SULFATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, DIMETHICONE, FRAGRANCE, PHENOXYETHANOL, METHYLPARABEN, PROPYLPARABEN, BUTYLPARABEN, IRON OXIDES

Purpose

Purpose:
Helps prevent sunburn.
Effective for sensitive skin easily prone to sun burns.

Warnings:
For external use only.
UV exposure from the sun increases the risk of skin cancer, premature skin aging and other skin damage.
It is important to decrease UV exposure by limiting time in the sun, wearing protective clothing, and using a sunscreen.
When using this product,  keep out of eyes. Rinse water to remove.
Stop use and ask a doctor, if rash or irritation develops and lasts.

Keep out of reach of children:
If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Indication and usage:
- Children under 6months of age: ask a doctor.
- Reapply as needed or after towel drying, swimming or perspiring.

Dosage and administration:
Apply liberally before sun exposure.

ATOMY SUN

OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52257-1204
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 4.5 mL
OCTISALATE OCTISALATE 3 mL
Zinc Oxide Zinc oxide 2.94 mL
titanium dioxide 1.49 mL

Inactive Ingredients

Ingredient Name Strength
water
CYCLOMETHICONE 5
GLYCERIN
DIPROPYLENE GLYCOL
cyclomethicone
PHENOXYETHANOL
aluminum hydroxide
aluminum stearate
METHYLPARABEN
PROPYLPARABEN
THYME OIL
ALTHAEA OFFICINALIS LEAF
MELISSA OFFICINALIS
CENTELLA ASIATICA
JASMINUM OFFICINALE FLOWER
BUTYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52257-1204-1 60 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-04-28


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