NDC 65734-740 Advance Acne Care

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:
Advance Acne Care
Product Type: [3]
Labeler Name: [5]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

Code Structure Chart

Product Details

What is NDC 65734-740?

The NDC code 65734-740 is assigned by the FDA to the product Advance Acne Care which is product labeled by Swabplus Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65734-740-00 1 kit in 1 carton * 24 applicator in 1 package (65734-741-24) / .15 ml in 1 applicator (65734-741-00) * 24 applicator in 1 package (65734-742-24) / .15 ml in 1 applicator (65734-742-00). 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 Advance Acne Care?

Do not use if label seal is broken prior to purchase.Keep swabs in original container when not in use. Treatment Swabs have a red color band.Use Cleansinh swab to cleanse the skin throughly before applying medication.Hold the swab vertically, with the color ring band tip upwards. Bend the tip at the color band to one side until it snaps. Medicine will flow to theother end.Cover the entire affected area with a thin layer 1 to 3 times daily. Discard swab after use.Each swab can be used on multipe pimples.Because excesssive drying of the skin may occur start with1 application daiky then gradually increase to 2 or 3 times daily if needed, or as direcvted by a doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every othr day. 

Which are Advance Acne Care UNII Codes?

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

Which are Advance Acne Care 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 Advance Acne Care?

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:

* 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".