NDC 76029-001 Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76029 - Active Release Techniques Llc
- 76029-001 - Pain Relief
Product Packages
NDC Code 76029-001-02
Package Description: 50 g in 1 CONTAINER
Product Details
What is NDC 76029-001?
What are the uses for Pain Relief?
Which are Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
Which are 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:
- ARGAN OIL (UNII: 4V59G5UW9X)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- RIBES NIGRUM SEED OIL (UNII: GKE1188837)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- TEA TREE OIL (UNII: VIF565UC2G)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".