NDC 54868-6381 Biclora
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6381 - Biclora
Product Characteristics
Product Packages
NDC Code 54868-6381-0
Package Description: 240 mL in 1 BOTTLE
Product Details
What is NDC 54868-6381?
What are the uses for Biclora?
Which are Biclora UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y)
- CHLOPHEDIANOL (UNII: 42C50P12AP) (Active Moiety)
- CHLORCYCLIZINE HYDROCHLORIDE (UNII: NPB7A7874U)
- CHLORCYCLIZINE (UNII: M26C4IP44P) (Active Moiety)
Which are Biclora 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Biclora?
- RxCUI: 1236710 - chlophedianol HCl 12.5 MG / chlorcyclizine HCl 12.5 MG in 5 mL Oral Solution
- RxCUI: 1236710 - chlophedianol hydrochloride 2.5 MG/ML / chlorcyclizine hydrochloride 2.5 MG/ML Oral Solution
- RxCUI: 1236710 - chlophedianol hydrochloride 12.5 MG / chlorcyclizine hydrochloride 12.5 MG per 5 ML Oral Solution
- RxCUI: 1358165 - Biclora 12.5 MG / 12.5 MG in 5 mL Oral Solution
- RxCUI: 1358165 - chlophedianol hydrochloride 2.5 MG/ML / chlorcyclizine hydrochloride 2.5 MG/ML Oral Solution [Biclora]
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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".