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  4. NDC Product Code: 52380-1272 Aplicare Antiseptic Chlorhexidine Gluconate

NDC 52380-1272 Aplicare Antiseptic Chlorhexidine Gluconate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52380-1272?
  4. Aplicare Antiseptic Chlorhexidine Gluconate Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52380-1272
Proprietary Name:
Aplicare Antiseptic Chlorhexidine Gluconate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aplicare, Inc.
Labeler Code:
52380
Product Label ID:
65f87900-8d23-4fb3-be44-1d116aedac78
Start Marketing Date: [9]
09-01-1998
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 52380-1272?

The NDC code 52380-1272 is assigned by the FDA to the product Aplicare Antiseptic Chlorhexidine Gluconate which is product labeled by Aplicare, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 52380-1272-4 118 ml in 1 bottle , 52380-1272-6 473 ml in 1 bottle , 52380-1272-7 946 ml in 1 bottle , 52380-1272-8 237 ml in 1 bottle , 52380-1272-9 3800 ml in 1 bottle . 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 Aplicare Antiseptic Chlorhexidine Gluconate?

Surgical hand scrubwet hands and forearms under running water for 30 secondsscrub for 3 minutes with about 5 mL of product with or without a wet brush, paying close attention to the nails, cuticles and interdigital spacesrinse thoroughly under running water for 30 secondsdry thoroughlyHealthcare personnel handwashwet hands with waterdispense about 5 mL of product into cupped hands and wash in a vigorous manner for 15 secondsrinse and dry thoroughlyPatient preoperative skin preparationapply product liberally to surgical site and swab for at least 2 minutesdry with a sterile towelrepeat procedure for an additional 2 minutes and dry with a sterile towelSkin wound and general cleansingthoroughly rinse the area to be cleaned with waterapply the minimum amount of product necessary to cover the skin or wound area and wash gentlyrinse again thoroughly

Which are Aplicare Antiseptic Chlorhexidine Gluconate UNII Codes?

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

Which are Aplicare Antiseptic Chlorhexidine Gluconate 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 Aplicare Antiseptic Chlorhexidine Gluconate?

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: 211365 - chlorhexidine gluconate 4 % Medicated Liquid Soap
  • RxCUI: 211365 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap
  • RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Surgical Scrub

* 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".