NDC 61577-7050 Sombra Cbd Warm Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61577 - Sombra Cosmetics Inc
- 61577-7050 - Sombra Cbd Warm Therapy
Product Packages
NDC Code 61577-7050-2
Package Description: 56.7 g in 1 BOTTLE, PUMP
NDC Code 61577-7050-4
Package Description: 113.4 g in 1 BOTTLE, PUMP
Product Details
What is NDC 61577-7050?
What are the uses for Sombra Cbd Warm Therapy?
Which are Sombra Cbd Warm Therapy 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 Sombra Cbd Warm Therapy 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)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- WATER (UNII: 059QF0KO0R)
- CAPSAICIN (UNII: S07O44R1ZM)
- GRAPEFRUIT SEED OIL (UNII: 598D944HOL)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
- ROSA CENTIFOLIA FLOWER OIL (UNII: H32V31VMWY)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- GLYCERIN (UNII: PDC6A3C0OX)
- WITCH HAZEL (UNII: 101I4J0U34)
- YUCCA SCHIDIGERA ROOT (UNII: E2H9ET15AT)
- ORANGE PEEL (UNII: TI9T76XD44)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CANNABIDIOL (UNII: 19GBJ60SN5)
* 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".