SKINUVA SCAR PLUS- zinc oxide cream 
MD Medical Designs, Inc.

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Skinuva® Scar plus

Drug Facts

Active ingredientsPurpose*
*
Data on file
Zinc Oxide 10%Sunscreen
Dosage FormCream

Uses

Helps prevent sunburn. If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only.

Do not use on damaged/broken skin or open wounds.

When using this product keep out of eyes. If contact occurs, rinse eyes thoroughly with plenty of water to remove. If swallowed immediately seek medical advice and show container or label.

Stop use and ask a doctor if rash or irritation occurs.

Keep out of reach of children.

Directions

Make sure the affected area is clean and dry. Apply a thin film over the affected area twice a day, morning and night. Wait 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor. See insert for detailed instructions.

Other information

Do not use if inner seal is broken. Store at room temperature. Avoid excessive heat.

Inactive ingredients

Water/Aqua, Dimethicone, Dimethiconol, Cyclopentasiloxane, Dimethicone Crosspolymer, Butylene Glycol, Glycerin, Diethylhexyl 2,6-Naphthalate, Dimethicone/PEG-10/15 Crosspolymer, Tetrahexyldecyl Ascorbate, Centella Asiatica Extract, Diphenylsiloxy Phenyl Trimethicone, Dimethicone/Phenyl Vinyl Dimethicone Crosspolymer, Phenoxyethanol, Ethylhexylglycerin, Sodium Chloride, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Sodium Hyaluronate, Aloe Barbadensis Leaf Juice, sh-Polypeptide-1, Tocopherol, sh-Polypeptide-6, sh-Polypeptide-5

Dist. by: MD Medical Designs, Inc.
Beverly Hills, CA 90210

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton

NDC: 82350-352-30

SKINUVA®
scar+

BROAD SPECTRUM SPF 30

Scar photoaging defense cream using
highly selective growth factors with
Zinc Oxide mineral sunscreen

Developed and tested
by physicians

30 mL / 1 fl. oz e

Principal Display Panel - 30 mL Bottle Carton
SKINUVA SCAR PLUS 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82350-352
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide0.1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Dimethicone (UNII: 92RU3N3Y1O)  
Cyclomethicone 5 (UNII: 0THT5PCI0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Glycerin (UNII: PDC6A3C0OX)  
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)  
Dimethicone/PEG-10/15 Crosspolymer (UNII: 21AS8B1BSS)  
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)  
Centella Asiatica Triterpenoids (UNII: 4YS74Q4G4J)  
Diphenylsiloxy Phenyl Trimethicone (UNII: I445L28B12)  
Dimethicone/Phenyl Vinyl Dimethicone Crosspolymer (UNII: ST6ZC4KVH2)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Sodium Chloride (UNII: 451W47IQ8X)  
Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone (UNII: 25G622K2RA)  
Hyaluronate Sodium (UNII: YSE9PPT4TH)  
Aloe Vera Leaf (UNII: ZY81Z83H0X)  
BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)  
Tocopherol (UNII: R0ZB2556P8)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Interleukin-10 (UNII: 9SC4O216V9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82350-352-151 in 1 CARTON06/30/2022
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:82350-352-301 in 1 CARTON06/30/2022
230 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM02006/30/2022
Labeler - MD Medical Designs, Inc. (094586004)

Revised: 1/2024
Document Id: e4c56b6d-c65f-4a9e-90b1-17841a18f6ab
Set id: 5fcad8c3-a268-4966-b0a9-6cd2c7afd3b7
Version: 2
Effective Time: 20240112
 
MD Medical Designs, Inc.