NDC 61577-6200 Provault Muscle Cream Cbd
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61577-6200?
What are the uses for Provault Muscle Cream Cbd?
Which are Provault Muscle Cream Cbd UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Provault Muscle Cream Cbd 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)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- TOCOPHEROL (UNII: R0ZB2556P8)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- SHEA BUTTER (UNII: K49155WL9Y)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- LEMON OIL (UNII: I9GRO824LL)
- CHAMOMILE (UNII: FGL3685T2X)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- HEMP (UNII: TD1MUT01Q7)
- MENTHA ARVENSIS FLOWER OIL (UNII: Q129Z1W6Y2)
- ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- CAPRYLIC/CAPRIC/LINOLEIC TRIGLYCERIDE (UNII: U73D397055)
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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".