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  4. NDC Product Code: 43749-112 Natures Choice Baby

NDC 43749-112 Natures Choice Baby

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43749-112?
  4. Natures Choice Baby Uses
  5. Active Ingredients UNII Codes
  6. 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:
43749-112
Proprietary Name:
Natures Choice Baby
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unipack, Inc.
Labeler Code:
43749
Product Label ID:
ba1ee906-1854-441c-b05d-dd6ca55b1a72
Start Marketing Date: [9]
06-07-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43749-112?

The NDC code 43749-112 is assigned by the FDA to the product Natures Choice Baby which is product labeled by Unipack, Inc.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 43749-112-05 50 g in 1 bottle , 43749-112-06 100 g in 1 bottle , 43749-112-07 113 g in 1 bottle , 43749-112-09 116 g in 1 bottle , 43749-112-10 368 g in 1 bottle , 43749-112-11 396 g in 1 bottle , 43749-112-14 424 g in 1 bottle , 43749-112-15 624 g 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 Natures Choice Baby?

UsesIt helps to absorb excess moisture, keeps the baby’s skin dry and soft for ultimate comfort.

Which are Natures Choice Baby UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Natures Choice Baby?

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".