NDC 24909-702 Cbd Clinic - Mild To Moderate Muscle And Joint Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24909 - Aidance Skincare & Topical Solutions, Llc
- 24909-702 - Cbd Clinic - Mild To Moderate Muscle And Joint Pain Relief
Product Packages
NDC Code 24909-702-44
Package Description: 44 g in 1 JAR
Product Details
What is NDC 24909-702?
What are the uses for Cbd Clinic - Mild To Moderate Muscle And Joint Pain Relief?
Which are Cbd Clinic - Mild To Moderate Muscle And Joint Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Cbd Clinic - Mild To Moderate Muscle And Joint 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:
- ARNICA MONTANA (UNII: O80TY208ZW)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CLOVE OIL (UNII: 578389D6D0)
- COTTONSEED OIL (UNII: H3E878020N)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- HEMP (UNII: TD1MUT01Q7)
- JOJOBA OIL (UNII: 724GKU717M)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SHEA BUTTER (UNII: K49155WL9Y)
- SILVER OXIDE (UNII: 897WUN6G6T)
- SORBIC ACID (UNII: X045WJ989B)
- TEA TREE OIL (UNII: VIF565UC2G)
- WATER (UNII: 059QF0KO0R)
- WHITE WAX (UNII: 7G1J5DA97F)
- ZINC OXIDE (UNII: SOI2LOH54Z)
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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".