NDC 81239-100 Baird Good Night

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:
81239-100
Proprietary Name:
Baird Good Night
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jk Inspir Co., Ltd
Labeler Code:
81239
Start Marketing Date: [9]
12-03-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81239-100-02

Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE (81239-100-01)

Product Details

What is NDC 81239-100?

The NDC code 81239-100 is assigned by the FDA to the product Baird Good Night which is product labeled by Jk Inspir Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81239-100-02 1 tube in 1 carton / 100 g in 1 tube (81239-100-01). 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 Baird Good Night?

Adults and children 2 years of age and olderBrush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.Children 2 to 6 yearsUse only a pea sized amount and supervise child’s brushing and rinsing (to minimize swallowing).Children under 2 yearsAsk a dentist or physician

What is the NDC to RxNorm Crosswalk for Baird Good Night?

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".