NDC 58133-800 Real Time Pain Relief Select Plus Hemp Oil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58133 - Cosmetic Specialty Labs, Inc.
- 58133-800 - Real Time Pain Relief Select Plus Hemp Oil
Product Packages
NDC Code 58133-800-03
Package Description: 88 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 58133-800?
What are the uses for Real Time Pain Relief Select Plus Hemp Oil?
Which are Real Time Pain Relief Select Plus Hemp Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
Which are Real Time Pain Relief Select Plus Hemp Oil 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)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TRIETHANOLAMINE TRIS(DIHYDROGEN PHOSPHATE) (UNII: 36YHT392ID)
- CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- RUBUS IDAEUS SEED (UNII: M3CL7US2ZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- HEMP (UNII: TD1MUT01Q7)
- CAPSICUM FRUTESCENS WHOLE (UNII: 6XJX33L87P)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MENTHOL (UNII: L7T10EIP3A)
- CHAMOMILE (UNII: FGL3685T2X)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- CORIANDRUM SATIVUM WHOLE (UNII: 740M8BF6EF)
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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".