NDC 48951-1148 Arnica Nettle Burn And Bite
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy Inc.
- 48951-1148 - Arnica Nettle Burn And Bite
Product Packages
NDC Code 48951-1148-5
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 48951-1148?
What are the uses for Arnica Nettle Burn And Bite?
Which are Arnica Nettle Burn And Bite UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N)
- THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- LARIX DECIDUA RESIN (UNII: AD8LJ73GQF)
- LARIX DECIDUA RESIN (UNII: AD8LJ73GQF) (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 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)
* 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".