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  4. NDC Product Code: 70512-100 Clotrimazole Cream 1%

NDC 70512-100 Clotrimazole Cream 1%

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70512-100?
  4. Clotrimazole Cream 1% Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70512-100
Proprietary Name:
Clotrimazole Cream 1%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sola Pharmaceuticals
Labeler Code:
70512
Product Label ID:
a3424c66-68ee-0631-e053-2995a90a3e7a
Start Marketing Date: [9]
04-14-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70512-100-15

Package Description: 1 TUBE in 1 CARTON / 14.2 g in 1 TUBE

NDC Code 70512-100-30

Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE

Price per Unit: $0.08818 per GM

Product Details

What is NDC 70512-100?

The NDC code 70512-100 is assigned by the FDA to the product Clotrimazole Cream 1% which is product labeled by Sola Pharmaceuticals. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70512-100-15 1 tube in 1 carton / 14.2 g in 1 tube, 70512-100-30 1 tube in 1 carton / 30 g in 1 tube. 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 Clotrimazole Cream 1%?

Clean the affected area and dry thoroughly. Apply a layer of cream over the affected area twice daily morning and night or as directed by doctor.Supervise children in the use of this product.For athlete's foot pay special attention to the spaces between toes. Wear well fitting ventilated shoes and change shoes and socks at least once daily.For athlete's foot and ringworm use daily for 4 weeks.For jock itch use daily for 2 weeks.If condition persist longer consult a doctor.This product is not effective on scalp or nails.

Which are Clotrimazole Cream 1% UNII Codes?

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

Which are Clotrimazole Cream 1% 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 Clotrimazole Cream 1%?

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:

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Patient Education

Clotrimazole Topical


Topical clotrimazole is used to treat tinea corporis (ringworm; fungal skin infection that causes a red scaly rash on different parts of the body), tinea cruris (jock itch; fungal infection of the skin in the groin or buttocks), and tinea pedis (athlete's foot; fungal infection of the skin on the feet and between the toes). Clotrimazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection.
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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".