NDC 43846-0037 Chafe Rescue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43846 - Peaceful Mountain, Inc
- 43846-0037 - Chafe Rescue
Product Packages
NDC Code 43846-0037-1
Package Description: 7 g in 1 PACKET
Product Details
What is NDC 43846-0037?
What are the uses for Chafe Rescue?
Which are Chafe Rescue UNII Codes?
The UNII codes for the active ingredients in this product are:
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- SULFURIC ACID (UNII: O40UQP6WCF)
- SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
Which are Chafe Rescue 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- COMFREY LEAF (UNII: DG4F8T839X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- MACADAMIA OIL (UNII: 515610SU8C)
- OREGANO (UNII: 0E5AT8T16U)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SOYBEAN OIL (UNII: 241ATL177A)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- SALIX ALBA BARK (UNII: 205MXS71H7)
* 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".