NDC 64479-201 Painpatrol Cbd Professional Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64479 - Smartscience Laboratories, Inc.
- 64479-201 - Painpatrol Cbd Professional Pain Relief
Product Packages
NDC Code 64479-201-11
Package Description: 88 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 64479-201?
What are the uses for Painpatrol Cbd Professional Pain Relief?
Which are Painpatrol Cbd Professional Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
Which are Painpatrol Cbd Professional Pain Relief 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA (UNII: O80TY208ZW)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLYCERIN (UNII: PDC6A3C0OX)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
* 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".