NDC 57955-0935 Warming Arthritic Pain And Joint Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57955-0935?
What are the uses for Warming Arthritic Pain And Joint Relief?
Which are Warming Arthritic Pain And Joint Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACTAEA SPICATA ROOT (UNII: 3FU86L9OS0)
- ACTAEA SPICATA ROOT (UNII: 3FU86L9OS0) (Active Moiety)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- FORMIC ACID (UNII: 0YIW783RG1)
- FORMIC ACID (UNII: 0YIW783RG1) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
Which are Warming Arthritic Pain And Joint Relief 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- JOJOBA OIL (UNII: 724GKU717M)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL TRICAPRYLATE (UNII: 6P92858988)
- CARYA OVATA BARK (UNII: X765CF609L)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPSICUM (UNII: 00UK7646FG)
- CHINESE CINNAMON LEAF OIL (UNII: 4U4V2F2E4Y)
- TANGERINE JUICE (UNII: 391Y6QJ4XR)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- CLOVE OIL (UNII: 578389D6D0)
- CAMPHOR LEAF OIL (UNII: 51D0RGY52V)
- CITRUS AURANTIUM FRUIT RIND (UNII: 055456JHI7)
- BITTER ORANGE OIL (UNII: 9TLV70SV6I)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- LACTIC ACID (UNII: 33X04XA5AT)
- VANILLIN (UNII: CHI530446X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".