NDC 69842-873 Cvs Pharmacy

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:
69842-873
Proprietary Name:
Cvs Pharmacy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
69842
Start Marketing Date: [9]
05-04-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CLEAR TO CLOUDY)

Code Structure Chart

Product Details

What is NDC 69842-873?

The NDC code 69842-873 is assigned by the FDA to the product Cvs Pharmacy which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69842-873-33 1 applicator in 1 carton / 5.9 ml in 1 applicator. 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 Cvs Pharmacy?

Adults and children 2 years of age or older: Apply to the skin. Benzocaine takes a minute to act. For insect bites, skin irritations, minor burns or sunburn, apply to the affected site not more than 3 to 4 times daily. Children under 2 years: consult physician.

Which are Cvs Pharmacy UNII Codes?

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

Which are Cvs Pharmacy 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 Cvs Pharmacy?

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: 2044375 - benzocaine 10 % / isopropyl alcohol 59 % Medicated Pad
  • RxCUI: 2044375 - benzocaine 100 MG/ML / isopropyl alcohol 0.59 ML/ML Medicated Pad

* 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".