OTC Medication Information: W.SKIN CICA PLUS REPAIR

W.SKIN CICA PLUS REPAIR- niacinamide and adenosine cream
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.

Niacinamide, Adenosine

Water, Butylene Glycol, Caprylic/Capric Triglyceride, Glycerin, Niacinamide, Betaine, Polyglyceryl-3 Methylglucose Distearate, Cetyl Alcohol, Butyrospermum Parkii (Shea) Butter, Glyceryl Stearate, Trehalose, Ammonium Acryloyldimethyltaurate/VP Copolymer, Glyceryl Caprylate, Glyceryl Stearate Citrate, Stearyl Alcohol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyisobutene, Chlorphenesin, Myristyl Alcohol, Allantoin, Fragrance, Panthenol, Adenosine, Lauryl Alcohol, Caprylyl/Capryl Glucoside, Sorbitan Oleate, Disodium EDTA, Centella Asiatica Extract, Acacia Senegal Gum, Citric Acid, Peat Water, Hydroxypropyl Methylcellulose, 1,2-Hexanediol, Portulaca Oleracea Extract, Pentylene Glycol, Caprylyl Glycol, Potassium Sorbate

Help to improve wrinkle and whitening

keep out of reach of the children

Take an appropriate amount of this product and spread it evenly on 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 CICA PLUS REPAIR
niacinamide, adenosine cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0010
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NIACINAMIDE (NIACINAMIDE) NIACINAMIDE 2 g in 100 mL
ADENOSINE (ADENOSINE) ADENOSINE 0.04 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
BUTYLENE GLYCOL
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:74997-0010-1 50 mL in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/25/2021
Labeler — J&J COMPANY (688995236)
Registrant — J&J COMPANY (688995236)
Establishment
Name Address ID/FEI Operations
J&J COMPANY 688995236 manufacture (74997-0010), label (74997-0010), pack (74997-0010)

Revised: 04/2021 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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