NDC 69512-700 Venia Patch Premium Pain Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69512 - Alivio Medical Products, Llc
- 69512-700 - Venia Patch
Product Packages
NDC Code 69512-700-05
Package Description: 10 PATCH in 1 BOX / 1 g in 1 PATCH
Product Details
What is NDC 69512-700?
What are the uses for Venia Patch Premium Pain Patch?
Which are Venia Patch Premium Pain Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Venia Patch Premium Pain Patch 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:
- ACRYLIC ACID (UNII: J94PBK7X8S)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- METHYL ACRYLATE (UNII: WC487PR91H)
- NONOXYNOL-30 (UNII: JJX07DG188)
- POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Venia Patch Premium Pain Patch?
- RxCUI: 1428948 - lidocaine 4 % / menthol 4 % Medicated Patch
- RxCUI: 1428948 - lidocaine 0.04 MG/MG / menthol 0.04 MG/MG Medicated Patch
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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".