OTC Medication Information: W.SKIN NATURAL FERMENTED GRAIN MASK SHEET

W.SKIN NATURAL FERMENTED GRAIN MASK SHEET- centella asiatica 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.

Centella Asiatica Extract

Water, Methylpropanediol, Glycerin, Caprylic/Capric Triglyceride, Niacinamide, Adenosine, Aspergillus/Rice Ferment Extract, Rice Ferment Filtrate (Sake), Oryza Sativa (Rice) Extract, Secale Cereale (Rye) Seed Extract, Hordeum Distichon (Barley) Extract, Vigna Radiata Seed Extract, Polygonum Fagopyrum (Buckwheat) Seed Extract, Galactomyces Ferment Filtrate, Acetyl Hexapeptide-8, Bifida Ferment Lysate, Centella Asiatica Extract, Allantoin, Squalane, Dimethicone, Polysorbate 80, Panthenol, Carbomer, SorbitanSesquioleate, Polyacrylamide, C13-14 Isoparaffin, Laureth-7 , Xanthan gum, Sodium Polyacrylate, Disodium EDTA, Tromethamine, Chlorphenesin, Hydroxyacetophenone, Fragrance.

Help to improve wrinkle and whitening

keep out of reach of the children

Put mask on the face for 10~20 minute and remove it. Tap remaining essence lightly to absorb it.

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 NATURAL FERMENTED GRAIN MASK SHEET
centella asiatica extract liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0025
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CENTELLA ASIATICA (CENTELLA ASIATICA) CENTELLA ASIATICA 0.01 g in 100 g
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:74997-0025-1 50 g in 1 POUCH 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 (74997-0025), label (74997-0025), pack (74997-0025)

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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