Label: MD CELL SOLUTION- niacinamide, panthenol, salicylic acid spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated July 21, 2016

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  • Active ingredients

    Niacinamide (0.3%)

    Panthenol (0.2%)

    Salicylic Acid (0.001%)

  • Purpose

    scalp tonic

    hair regrowth treatment

  • Keep out of reach of children

    - Do not swallow. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

  • Uses

    Helps restore damaged scalp and keep it moisturized after hair transplant. To give nutrition on hair follicle of the surgical site to help graft anchoring in hair transplant. Reduces scalp itching. To regrow hair on the top of the scalp

  • Warnings

    For external use only


    Do not use on damaged or broken scalp


    When using this product
    - Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.


    Stop use and ask doctor if rash or irritation on scalp develops and lasts.

    - Store at room temperature

  • Directions

    Spray on scalp hourly (recommended) after hair transplant more than three days to keep the area moist.

  • Inactive Ingredients

    Water, Glycerin, Butylene Glycol, Urtica Dioica (Nettle) Extract, Honey Extract, Betaine, sh-Polypeptide-9, Nelumbo Nucifera Flower Extract, Prunus Mume Fruit Extract, Copper Tripeptide-1, rh-Oligopeptide-1, rh-Polypeptide-3, Aloe Barbadensis Leaf Extract, Allantoin, Citric Acid, Paeonia Lactiflora Root Extract, Magnolia Kobus Branch/Flower/Leaf Extract, Lilium Candidum Flower Extract, Ipomoea Purpurea Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Fragaria Chiloensis (Strawberry) Fruit Extract, Vaccinium Myrtillus Fruit Extract, Phyllanthus Emblica Fruit Extract, Fragaria Vesca (Strawberry) Leaf Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Erythritol

  • MD CELL Solution

    md cell solution

  • INGREDIENTS AND APPEARANCE
    MD CELL SOLUTION 
    niacinamide, panthenol, salicylic acid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70834-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide0.003   in 100 mL
    Panthenol (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) Panthenol0.002   in 100 mL
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid0.00001   in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    URTICA DIOICA LEAF (UNII: X6M0DRN46Q)  
    HONEY (UNII: Y9H1V576FH)  
    Betaine (UNII: 3SCV180C9W)  
    NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)  
    PRUNUS MUME FRUIT (UNII: 639190I8CU)  
    PREZATIDE COPPER (UNII: 6BJQ43T1I9)  
    NEPIDERMIN (UNII: TZK30RF92W)  
    FIBROBLAST GROWTH FACTOR 7 (UNII: 9YXF283GP1)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Allantoin (UNII: 344S277G0Z)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    MAGNOLIA KOBUS FLOWERING TOP (UNII: X2725LP5TL)  
    LILIUM CANDIDUM FLOWER (UNII: COV655U2CJ)  
    IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O)  
    LOWBUSH BLUEBERRY (UNII: G90PX41VP0)  
    BLACKBERRY (UNII: 8A6OMU3I8L)  
    ACAI (UNII: 46AM2VJ0AW)  
    RASPBERRY (UNII: 4N14V5R27W)  
    BEACH STRAWBERRY (UNII: 98542F2TQS)  
    BILBERRY (UNII: 9P2U39H18W)  
    PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)  
    FRAGARIA VESCA LEAF (UNII: I14FE7JUBB)  
    CRANBERRY (UNII: 0MVO31Q3QS)  
    Erythritol (UNII: RA96B954X6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70834-102-021 in 1 PACKAGE07/22/2016
    1NDC:70834-102-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/22/2016
    Labeler - A Joint-stock Corporation GMC Holdings (689847352)
    Registrant - A Joint-stock Corporation GMC Holdings (689847352)
    Establishment
    NameAddressID/FEIBusiness Operations
    A Joint-stock Corporation GMC Holdings689847352manufacture(70834-102)