NDC 10237-907 Legatrin Pm

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:
10237-907
Proprietary Name:
Legatrin Pm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Church & Dwight Co., Inc.
Labeler Code:
10237
Start Marketing Date: [9]
10-01-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
OVAL (C48345)
Size(s):
17 MM
Imprint(s):
LEGATRIN
Score:
1

Product Packages

NDC Code 10237-907-50

Package Description: 1 BOTTLE in 1 CARTON / 50 TABLET in 1 BOTTLE

Product Details

What is NDC 10237-907?

The NDC code 10237-907 is assigned by the FDA to the product Legatrin Pm which is product labeled by Church & Dwight Co., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10237-907-50 1 bottle in 1 carton / 50 tablet 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 Legatrin Pm?

DirectionsDo not exceed recommended dosage.Adults and children 12 years of age and older1 caplet at bedtime as needed, or as directed by a doctorChildren under 12 yearsconsult a doctor

Which are Legatrin Pm UNII Codes?

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

Which are Legatrin Pm 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 Legatrin Pm?

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:
  • RxCUI: 1087607 - acetaminophen 500 MG / diphenhydrAMINE HCl 50 MG Oral Tablet
  • RxCUI: 1087607 - acetaminophen 500 MG / diphenhydramine hydrochloride 50 MG Oral Tablet
  • RxCUI: 1087607 - APAP 500 MG / diphenhydramine hydrochloride 50 MG Oral Tablet
  • RxCUI: 1087609 - Legatrin PM 500 MG / 50 MG Oral Tablet
  • RxCUI: 1087609 - acetaminophen 500 MG / diphenhydramine hydrochloride 50 MG Oral Tablet [Legatrin PM]

* Please review the disclaimer below.

Patient Education

Acetaminophen


Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.
[Learn More]


Diphenhydramine


Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is also used to relieve cough caused by minor throat or airway irritation. Diphenhydramine is also used to prevent and treat motion sickness, and to treat insomnia (difficulty falling asleep or staying asleep). Diphenhydramine is also used to control abnormal movements in people who have early stage parkinsonian syndrome (a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) or who are experiencing movement problems as a side effect of a medication. Diphenhydramine will relieve the symptoms of these conditions but will not treat the cause of the symptoms or speed recovery. Diphenhydramine should not be used to cause sleepiness in children. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
[Learn More]


* 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".