NDC 51316-938 Pain And Fever

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
51316-938
Proprietary Name:
Pain And Fever
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Labeler Code:
51316
Start Marketing Date: [9]
02-15-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Code Structure Chart

Product Details

What is NDC 51316-938?

The NDC code 51316-938 is assigned by the FDA to the product Pain And Fever 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 51316-938-04 1 bottle, plastic in 1 box / 118 ml in 1 bottle, plastic. 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 Pain And Fever?

This product does not contain directions or complete warnings for adult usedo not give more than directedshake well before usingmL= milliliter find the right dose on chart. If possible, use weight to dose; otherwise use ageuse only enclosed dosing cup. Do not use any other dosing device/if needed, repeat dose every 6-8 hoursdo not use more than 4 times a dayreplace original bottle cap to maintain child resistanceDosing Chart Weight (lb)Age (yr)Dose (mL)* under 24under 2ask a doctor 24-352-35 mL  36-474-5 7.5 ml 48-596-810 mL  60-719-1012.5 mL  72-951115 mL *or as directed by a doctor

Which are Pain And Fever UNII Codes?

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

Which are Pain And Fever 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:

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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".