NDC 48951-1218 Arnica Nettle Burn And Bite Special Order
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 48951-1218?
What are the uses for Arnica Nettle Burn And Bite Special Order?
Which are Arnica Nettle Burn And Bite Special Order UNII Codes?
The UNII codes for the active ingredients in this product are:
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- LARIX DECIDUA RESIN (UNII: AD8LJ73GQF)
- LARIX DECIDUA RESIN (UNII: AD8LJ73GQF) (Active Moiety)
- THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N)
- THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
Which are Arnica Nettle Burn And Bite Special Order 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)
- ALCOHOL (UNII: 3K9958V90M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAJUPUT OIL (UNII: J3TO6BUQ37)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- TEA TREE OIL (UNII: VIF565UC2G)
- THYME OIL (UNII: 2UK410MY6B)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
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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".