NDC 49638-104 Tylo Arthritis (acetaminophen)

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:
49638-104
Proprietary Name:
Tylo Arthritis (acetaminophen)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
America Medic & Science, Llc
Labeler Code:
49638
Start Marketing Date: [9]
01-17-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
8 MM
Score:
1

Product Packages

NDC Code 49638-104-30

Package Description: 1 BOTTLE in 1 CARTON / 30 TABLET, DELAYED RELEASE in 1 BOTTLE

Product Details

What is NDC 49638-104?

The NDC code 49638-104 is assigned by the FDA to the product Tylo Arthritis (acetaminophen) which is product labeled by America Medic & Science, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49638-104-30 1 bottle in 1 carton / 30 tablet, delayed release 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 Tylo Arthritis (acetaminophen)?

Do not take more than directed (see overdose warning).take 2 caplets every 8 hours with water.Swallow whole—do not crush, chew, split or dissolve.Do not take more than 6 caplets in 24 hours.Do not use for more than 10 days unless directed by a doctor.ChildrenUnder 18 years of age ask a doctor.

Which are Tylo Arthritis (acetaminophen) UNII Codes?

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

Which are Tylo Arthritis (acetaminophen) 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".