NDC 43846-0060 Arnica Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43846 - Peaceful Mountain, Inc.
- 43846-0060 - Arnica Plus
Product Details
What is NDC 43846-0060?
What are the uses for Arnica Plus?
Which are Arnica Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
Which are Arnica Plus 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:
- WATER (UNII: 059QF0KO0R)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- WHEY (UNII: 8617Z5FMF6)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- OREGANO (UNII: 0E5AT8T16U)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".