W.SKIN TRIPLE CARE SUN- ethylhexyl methoxycinnamate cream

W.SKIN TRIPLE CARE SUN by

Drug Labeling and Warnings

W.SKIN TRIPLE CARE SUN by is a Otc medication manufactured, distributed, or labeled by J&J COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethylhexyl Methoxycinnamate

INACTIVE INGREDIENT

Isoamyl p-Methoxycinnamate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Zinc Oxide, Propylene Glycol, Glycerin, Sodium Hyaluronate, Glyceryl Stearate, Glyceryl Stearate SE, Sorbitan Stearate, Sorbitan Sesquioleate, 1,2-Hexanediol, Polysorbate 60, Isopropyl Myristate, Caprylic/Capric Triglyceride, Cyclomethicone, Phenyl Trimethicone, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Adenosine, Beeswax

PURPOSE

It has a strong sun block and waterproof function. It contains a large amount of hyaluronic acid to prevent evaporation of moisture from the skin.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

At the end of skin care, take an appropriate amount and apply evenly over the skin

WARNINGS

If there are any abnormal symptoms or side effects such as red spots, swelling, or itching due to direct sunlight during or after using cosmetics. 2. Avoid using areas with wounds. 3. Precautions for storage and handling. 3.1) Keep out reach of children. 3.2) Keep it out of direct sunlight.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

W.SKIN TRIPLE CARE SUN 
ethylhexyl methoxycinnamate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74997-0014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74997-0014-1	60 g in 1 TUBE; Type 0: Not a Combination Product	05/08/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/08/2021

Labeler - J&J COMPANY (688995236)

Registrant - J&J COMPANY (688995236)

Establishment
Name	Address	ID/FEI	Business Operations
J&J COMPANY		688995236	manufacture(74997-0014) , label(74997-0014) , pack(74997-0014)