NDC 52925-312 Vcf Contraceptive

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:
Proprietary Name:
Vcf Contraceptive
Product Type: [3]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
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Product Details

What is NDC 52925-312?

The NDC code 52925-312 is assigned by the FDA to the product Vcf Contraceptive which is product labeled by Apothecus Pharmaceutical Corp. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 52925-312-06 17 g in 1 can , 52925-312-14 1 can in 1 box / 17 g in 1 can. 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 Vcf Contraceptive?

Before using this product, read the enclosed package insert for complete directions and informationinsert one applicator full of foam in the vagina no more than one hour before each act of intercourseif this product is used together with another contraceptive method, there will probably be better protection against pregnancyif douching is desired, always wait at least 6 hours after intercourse before douchingsee enclosed instructions for cleaning the applicator after each use

Which are Vcf Contraceptive UNII Codes?

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

Which are Vcf Contraceptive 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 Vcf Contraceptive?

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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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".