NDC 63029-811 Pediacare Gas Relief Drops Dye Free

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:
63029-811
Proprietary Name:
Pediacare Gas Relief Drops Dye Free
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
63029
Start Marketing Date: [9]
08-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
BERRY (C73365)

Code Structure Chart

Product Details

What is NDC 63029-811?

The NDC code 63029-811 is assigned by the FDA to the product Pediacare Gas Relief Drops Dye Free which is product labeled by Medtech Products Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63029-811-01 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper. 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 Pediacare Gas Relief Drops Dye Free?

Shake well before usingall dosages may be repeated as needed, after meals and at bedtimefill enclosed dropper to recommended dosage levelDose by weight or if weight information is not available, dose by age. dispense liquid slowly into baby’s mouth, toward inner cheekmay mix with 1 oz. of cool water, infant formula or other suitable liquidsclean dropper after each use and replace original capage (yr)weight (lb)doseinfants under 2under 240.3 mLchildren 2 and over24 and over0.6 mL

Which are Pediacare Gas Relief Drops Dye Free UNII Codes?

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

Which are Pediacare Gas Relief Drops Dye Free 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:

* 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".