NDC 61577-7500 Sombra Plus Cbd 500mg Cool Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61577 - Sombra Cosmetics Inc.
- 61577-7500 - Sombra Plus Cbd 500mg Cool Therapy
Product Packages
NDC Code 61577-7500-2
Package Description: 56.7 g in 1 JAR
NDC Code 61577-7500-4
Package Description: 113.4 g in 1 JAR
Product Details
What is NDC 61577-7500?
What are the uses for Sombra Plus Cbd 500mg Cool Therapy?
Which are Sombra Plus Cbd 500mg Cool Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Sombra Plus Cbd 500mg Cool 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)
- 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)
- LEMON OIL (UNII: I9GRO824LL)
- 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".