NDC 76312-002 Tricalm Extra Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76312 - Cosmederm Bioscience
- 76312-002 - Tricalm
Product Packages
NDC Code 76312-002-01
Package Description: 1 TUBE in 1 BOX / 55 mL in 1 TUBE
Product Details
What is NDC 76312-002?
What are the uses for Tricalm Extra Strength?
Which are Tricalm Extra Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ACETATE (UNII: 80EHD8I43D)
- ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)
Which are Tricalm Extra Strength 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- LACTIC ACID (UNII: 33X04XA5AT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
- STRONTIUM NITRATE (UNII: BDG873AQZL)
What is the NDC to RxNorm Crosswalk for Tricalm Extra Strength?
- RxCUI: 1657022 - aluminum acetate 0.3 % Topical Spray
- RxCUI: 1657022 - aluminum acetate 3 MG/ML Topical Spray
- RxCUI: 1657025 - TRICALM 0.3 % Topical Spray
- RxCUI: 1657025 - aluminum acetate 3 MG/ML Topical Spray [Tricalm]
- RxCUI: 1657025 - TriCalm 0.3 % Topical Spray
* 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".