NDC 69842-212 Honey Lemon Cough Drops

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:
69842-212
Proprietary Name:
Honey Lemon Cough Drops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy, Inc
Labeler Code:
69842
Start Marketing Date: [9]
05-25-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
OVAL (C48345)
Size(s):
17 MM
Imprint(s):
NONE
Flavor(s):
HONEY (C73394)
LEMON (C73396)

Product Packages

NDC Code 69842-212-01

Package Description: 150 PASTILLE in 1 BAG

Product Details

What is NDC 69842-212?

The NDC code 69842-212 is assigned by the FDA to the product Honey Lemon Cough Drops which is product labeled by Cvs Pharmacy, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69842-212-01 150 pastille in 1 bag . 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 Honey Lemon Cough Drops?

Uses Temporarily relieves:cough as may occur with cold or inhaled irritantsocassional minor irritations and sore throat

Which are Honey Lemon Cough Drops UNII Codes?

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

Which are Honey Lemon Cough Drops 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 Honey Lemon Cough Drops?

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 code indicates a single concept unique identifier (RXCUI) is 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".