NDC 51824-081 Careall Non-aspirin Pm Extra Strength

Acetaminophen, Diphenhydramine Hcl

NDC Product Code 51824-081

NDC CODE: 51824-081

Proprietary Name: Careall Non-aspirin Pm Extra Strength What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Acetaminophen, Diphenhydramine Hcl What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.

Product Characteristics

BLUE (C48333)
Shape: CAPSULE (C48336)
16 MM
Score: 1

NDC Code Structure

  • 51824 - New World Imports, Inc

NDC 51824-081-50

Package Description: 50 TABLET in 1 BOTTLE

NDC Product Information

Careall Non-aspirin Pm Extra Strength with NDC 51824-081 is a a human over the counter drug product labeled by New World Imports, Inc. The generic name of Careall Non-aspirin Pm Extra Strength is acetaminophen, diphenhydramine hcl. The product's dosage form is tablet and is administered via oral form.

Labeler Name: New World Imports, Inc

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Careall Non-aspirin Pm Extra Strength Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACETAMINOPHEN 500 mg/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: New World Imports, Inc
Labeler Code: 51824
FDA Application Number: part343 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-20-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Careall Non-aspirin Pm Extra Strength Product Label Images

Careall Non-aspirin Pm Extra Strength Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Acetaminophen 500mg Diphenhydramine HCl 25mg


Pain relieverNightime sleep aid

Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental overdose, contact a doctor or Poison Control Center (1-800-222-1222) right away.  Prompt Medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.


Temporarily relieves occasional headaches and minor aches and pains with accompanying sleeplessness


  • Liver Warning: This product contains Acetaminophen. Severe liver damage may occur if you take • More than 4000 mg of acetaminophen in 24 hours • with other drugs containing acetaminophen • 3 or more alcoholic drinks every day while using this product.Allergy Alert:Acetaminophen may cause severe skin reactions.  Symptoms may include: skin reddening, blisters, rash.  If a skin reaction occurs, stop use and seek medical help right away.Do not use:with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.with any other product containing diphenhydramine, even one used on skinin children under 12 years of ageif you have even had an allergic reaction to this product or any of its ingredientsAsk a doctor before use if youhaveliver diseasea breathing problem such as emphysema or chronic bronchitistrouble urinating due to an enlarged prostate glandglaucomaAsk a doctor or pharmacist before use if youaretaking the blood thinning drug warfarintaking sedatives or tranquilizersWhen using this product •drowsiness will occur •do not drive a motor vehicle or operate machinery •avoid alcoholic drinksStop use and ask a doctor if •sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness •pain gets worse or last for more than 10 days. •fever gets worse or last for more than 3 days •redness or swelling are present •new symptoms occur.  These could be signs of a serious condition.If pregnant or breast-feeding, ask a health professional before use.


Do not use more than directed.  (see overdose warning)Adults and children 12 years of age and older: Take 2 caplets at bedtime.  Do not take more than 2 caplets in 24 hoursChildren under 12 years: do not use

Inactive Ingredients

Croscarmellose sodium, FD and C blue #1 aluminum lake, hypromellose, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, silicon dioxide, stearic acid, titanium dioxide.  May contain: carnauba wax, FD and C Blue #2 aluminum lake, polysorbate 80

* Please review the disclaimer below.