NDC 76071-1001 Stem Cell Renew
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76071-1001?
What are the uses for Stem Cell Renew?
Which are Stem Cell Renew UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Stem Cell Renew 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:
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PREZATIDE COPPER ACETATE (UNII: A3LEI4P1NB)
- PENTIGETIDE (UNII: YG3J18T1UX)
- ACETYL HEXAPEPTIDE-3 (UNII: L4EL31FWIL)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- BETAINE (UNII: 3SCV180C9W)
- SORBITAN (UNII: 6O92ICV9RU)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- ARGININE (UNII: 94ZLA3W45F)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ALLANTOIN (UNII: 344S277G0Z)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HONEY (UNII: Y9H1V576FH)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- CERAMIDE 3 (UNII: 4370DF050B)
- CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
* 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".