NDC 70834-102 Md Cell Solution
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70834-102?
What are the uses for Md Cell Solution?
Which are Md Cell Solution UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Md Cell Solution Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".