NDC 24385-439 Caldyphen Clear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24385 - Amerisource Bergen
- 24385-439 - Caldyphen Clear
Product Packages
NDC Code 24385-439-30
Package Description: 177 mL in 1 BOTTLE, PLASTIC
Price per Unit: $0.01339 per ML
Product Details
What is NDC 24385-439?
What are the uses for Caldyphen Clear?
Which are Caldyphen Clear UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
- ZINC ACETATE (UNII: FM5526K07A)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Caldyphen Clear 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:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYPROPYL METHYLCELLULOSE E5 [II] (UNII: R75537T0T4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Caldyphen Clear?
- RxCUI: 1234546 - pramoxine HCl 1 % / zinc acetate 0.1 % Topical Lotion
- RxCUI: 1234546 - pramoxine hydrochloride 10 MG/ML / zinc acetate 1 MG/ML Topical Lotion
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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".