Label: MD CELL SOLUTION- niacinamide, panthenol, salicylic acid spray
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Contains inactivated NDC Code(s)
NDC Code(s): 70834-102-01, 70834-102-02 - Packager: A Joint-stock Corporation GMC Holdings
- 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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- Directions
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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
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INGREDIENTS AND APPEARANCE
MD CELL SOLUTION
niacinamide, panthenol, salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70834-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.003 in 100 mL Panthenol (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) Panthenol 0.002 in 100 mL Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid 0.00001 in 100 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:70834-102-02 1 in 1 PACKAGE 07/22/2016 1 NDC:70834-102-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/22/2016 Labeler - A Joint-stock Corporation GMC Holdings (689847352) Registrant - A Joint-stock Corporation GMC Holdings (689847352) Establishment Name Address ID/FEI Business Operations A Joint-stock Corporation GMC Holdings 689847352 manufacture(70834-102)