NDC 43846-0073 Muscle Ice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 43846-0073?
What are the uses for Muscle Ice?
Which are Muscle Ice UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Muscle Ice 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:
- MENTHOL (UNII: L7T10EIP3A)
- WATER (UNII: 059QF0KO0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SPANISH THYME OIL (UNII: U14667H96E)
- GINGER OIL (UNII: SAS9Z1SVUK)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- HYPERICUM OIL (UNII: OZU2FC70HY)
- ALCOHOL (UNII: 3K9958V90M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
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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".