NDC 69170-104 Muscle And Joint Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69170 - Naturalrx Llc
- 69170-104 - Muscle And Joint Relief
Product Packages
NDC Code 69170-104-14
Package Description: 118 mL in 1 TUBE
Product Details
What is NDC 69170-104?
What are the uses for Muscle And Joint Relief?
Which are Muscle And Joint Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- EMU OIL (UNII: 344821WD61)
- EMU OIL (UNII: 344821WD61) (Active Moiety)
Which are Muscle 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)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ALMOND OIL (UNII: 66YXD4DKO9)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- STEARETH-20 (UNII: L0Q8IK9E08)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SHEA BUTTER (UNII: K49155WL9Y)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
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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".