NDC 73356-050 Relivbliss
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73356 - Etrading Pier Llc
- 73356-050 - Relivbliss
Product Packages
NDC Code 73356-050-50
Package Description: 74 mL in 1 TUBE
Product Details
What is NDC 73356-050?
What are the uses for Relivbliss?
Which are Relivbliss UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Relivbliss 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:
- ALLANTOIN (UNII: 344S277G0Z)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PAPRIKA (UNII: X72Z47861V)
- EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
- CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- ALCOHOL (UNII: 3K9958V90M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPANEDIOL (UNII: 5965N8W85T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".