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Atomy Sunscreen Beige

FULL PRESCRIBING INFORMATION: CONTENTS*

ACTIVE INGREDIENT
INACTIVE INGREDIENT
PURPOSE
WARNINGS
KEEP OUT OF REACH OF CHILDREN
INDICATIONS AND USAGE
DOSAGE AND ADMINISTRATION
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: Octinoxate, Octisalate, Zinc Oxide, Titanium Dioxide

INACTIVE INGREDIENT

Inactive Ingredients
WATER, CYCLOPENTASILOXANE, GLYCERIN, DIPROPYLENE GLYCOL, PEG-10 DIMETHICONE, CYCLOMETHICONE, DISTEARDIMONIUM HECTORITE, THYMUS VULGARIS (THYME) OIL, CAMELLIA SINENSIS LEAF EXTRACT, MELISSA OFFICINALIS EXTRACT, ALTHAEA OFFICINALIS LEAF/ROOT EXTRACT, PERILLA OCYMOIDES LEAF EXTRACT, CENTELLA ASIATICA EXTRACT, BORAGO OFFICINALIS EXTRACT, JASMINUM OFFICINALE (JASMINE) EXTRACT, MAGNESIUM SULFATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, ALUMINUM HYDROXIDE,
ALUMINUM STEARATE, METHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, FRAGRANCE, PHENOXYETHANOL, METHYLPARABEN, PROPYLPARABEN, BUTYLPARABEN

PURPOSE

Purpose: SUNSCREEN

WARNINGS

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 with 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.

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

Directions
Apply liberally before sun exposure.
Children under 6 months of age: ask a doctor
Reapply as needed or after swimming, perspiring, or towel drying.

DOSAGE AND ADMINISTRATION

Directions
Apply liberally before sun exposure.
Children under 6 months of age: ask a doctor
Reapply as needed or after swimming, perspiring, or towel drying.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

Atomy Sunscreen Beige

Octinoxate, Octisalate, Zinc Oxide, Titanium Dioxide CREAM

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:52257-1210
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE OCTINOXATE		4.08 mg
OCTISALATE OCTISALATE		2.7 mg
Zinc Oxide Zinc oxide		8.06 mg
titanium dioxide		2.92 mg

Inactive Ingredients
Ingredient Name	Strength
water
GLYCERIN

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:52257-1210-1	60 in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
part	part352	2013-02-01

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!