NDC 67091-120 Childrens Pain Relief 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:
67091-120
Proprietary Name:
Childrens Pain Relief Dye-free
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Winco Foods, Llc
Labeler Code:
67091
Start Marketing Date: [9]
12-12-2014
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 67091-120-18

Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE

Product Details

What is NDC 67091-120?

The NDC code 67091-120 is assigned by the FDA to the product Childrens Pain Relief Dye-free which is product labeled by Winco Foods, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67091-120-18 1 bottle in 1 carton / 118 ml 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 Childrens Pain Relief Dye-free?

Do not give more than directed (see overdose warning)shake well before usethis product does not contain directions or complete warnings for adult doseuse only enclosed dosing cuprepeat dose every 4 hours while symptoms lastdo not give more than 5 times in 24 hoursfind right dose on chart below. If possible, use weight to dose; otherwise, use age. Weight (lb) Age (yr) Dose (mL) under 24 lbs under 2 years ask a doctor 24-35 lbs 2-3 years 5 mL 36-47 lbs 4-5 years 7.5 mL 48 - 59 lbs 6-8 years 10 mL 60 - 71 lbs 9-10 years 12.5 mL 72 - 95 lbs 11 years 15 mL

Which are Childrens Pain Relief Dye-free UNII Codes?

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

Which are Childrens Pain Relief 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:

What is the NDC to RxNorm Crosswalk for Childrens Pain Relief Dye-free?

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".