NDC 24385-439 Caldyphen Clear

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
24385-439
Proprietary Name:
Caldyphen Clear
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amerisource Bergen
Labeler Code:
24385
Start Marketing Date: [9]
01-01-2008
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

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?

The NDC code 24385-439 is assigned by the FDA to the product Caldyphen Clear which is product labeled by Amerisource Bergen. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24385-439-30 177 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Caldyphen Clear?

Adults and children 2 yrs. of age and older. Shake well before using. cleanse the skin with soap and water. Let dry before each use. apply lotion to the affected area using cotton or soft cloth, not more than 3 to 4 times daily as needed for comfort.children unedr 2 yrs. of age. Consult a doctor before use.

Which are Caldyphen Clear UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Caldyphen Clear?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[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".