NDC 44911-0304 Joint Pain And Stiffness Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44911 - Energique, Inc.
- 44911-0304 - Joint Pain And Stiffness Relief
Product Packages
NDC Code 44911-0304-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 44911-0304?
What are the uses for Joint Pain And Stiffness Relief?
Which are Joint Pain And Stiffness Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SARSAPARILLA (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
Which are Joint Pain And Stiffness 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- LARREA TRIDENTATA TOP (UNII: PK0TXD049P)
- COMFREY LEAF (UNII: DG4F8T839X)
- CROTON LECHLERI RESIN (UNII: GGG6W25C63)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- SILVER (UNII: 3M4G523W1G)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- PHYTOLACCA AMERICANA FRUIT (UNII: WE63661499)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- WHEY (UNII: 8617Z5FMF6)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- ACHILLEA MILLEFOLIUM FLOWER (UNII: YQR8R0SQEA)
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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".