NDC 50795-2001 U-max Multi Bb
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 50795-2001?
What are the uses for U-max Multi Bb?
Which are U-max Multi Bb UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are U-max Multi Bb 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)
- MACADAMIA NUT (UNII: Y5432RGW8N)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- XANTHIUM STRUMARIUM FRUIT (UNII: TN770YC17C)
- SOLANUM LYCOPERSICUM (UNII: 0243Q4990L)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- BANANA (UNII: 4AJZ4765R9)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- JOJOBA OIL (UNII: 724GKU717M)
- LAMINARIA JAPONICA (UNII: WE98HW412B)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- SHEA BUTTER (UNII: K49155WL9Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
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[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".