NDC 73247-392 Zionodil 100
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73247 - Bodyshphere, Llc
- 73247-392 - Zionodil 100
Product Characteristics
Product Packages
NDC Code 73247-392-06
Package Description: 177 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 73247-392?
What are the uses for Zionodil 100?
Which are Zionodil 100 UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Zionodil 100 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- TRICAPRILIN (UNII: 6P92858988)
- CHONDROITIN 6-SULFATE (UNII: 7LWQ6472SP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EMU OIL (UNII: 344821WD61)
- WATER (UNII: 059QF0KO0R)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- TROLAMINE (UNII: 9O3K93S3TK)
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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".