NDC 59279-502 Solv X

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:
59279-502
Proprietary Name:
Solv X
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
59279
Start Marketing Date: [9]
01-01-1994
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 59279-502?

The NDC code 59279-502 is assigned by the FDA to the product Solv X which is product labeled by Mediceutical Laboratories, Ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 59279-502-06 .18 l in 1 bottle, plastic , 59279-502-12 .36 l in 1 bottle, plastic , 59279-502-33 1 l 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 Solv X?

For best results use daily or until condition is under control or as directed by a physician.For maximum control use every time you shampoo.Wet hair, massage liberal amount of Solv-XTM onto the scalp and through the hairThoroughly rinse and repeat if desiredApply TherapeuticTM Scalp and Hair Treatment Rinse for 1-2 minutes, thoroughly rinse.Consult your Salon professional for additional Mediceuticals® scalp and hair treatments specifically tailored for your condition.

Which are Solv X UNII Codes?

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

Which are Solv X 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 Solv X?

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".