OTC Medication Information: W.SKIN HYALURONIC TONER

W.SKIN HYALURONIC TONER- hyaluronate sodium liquid
J&J COMPANY

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Ethylhexyl Methoxycinnamate

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

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 the children

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

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.

for external use only

label
(click image for full-size original)

W.SKIN HYALURONIC TONER
sodium hyaluronate liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0019
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYALURONATE SODIUM (HYALURONIC ACID) HYALURONATE SODIUM 0.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:74997-0019-1 250 mL in 1 BOTTLE None
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 Operations
J&J COMPANY 688995236 manufacture (74997-0019), label (74997-0019), pack (74997-0019)

Revised: 05/2021 J&J COMPANY

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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