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NDC 41250-0966-47 arthritis pain relief 650 mg/1 Details
arthritis pain relief 650 mg/1
arthritis pain relief is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution Inc. The primary component is ACETAMINOPHEN.
MedlinePlus Drug Summary
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.
Related Packages: 41250-0966-47Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Acetaminophen
Product Information
| NDC | 41250-0966 |
|---|---|
| Product ID | 41250-966_a80c0c5f-8bf9-4d1f-99cf-efd421d3db1a |
| Associated GPIs | 64100010000510 64200010000420 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | arthritis pain relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Acetaminophen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 650 |
| Active Ingredient Units | mg/1 |
| Substance Name | ACETAMINOPHEN |
| Labeler Name | Meijer Distribution Inc |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075077 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 41250-0966-47 (41250096647)
| NDC Package Code | 41250-966-47 |
|---|---|
| Billing NDC | 41250096647 |
| Package | 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-966-47) |
| Marketing Start Date | 2007-09-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL c388f3a5-03bb-4fed-b81a-bb876bc260f0 Details
Uses
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
- •
- more than 6 caplets in 24 hours, which is the maximum daily amount
- •
- with other drugs containing acetaminophen
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- 3 or more alcoholic drinks every day while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
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- skin reddening
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- blisters
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- rash
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
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- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
- •
- if you are allergic to acetaminophen or any of the inactive ingredients in this product
Directions
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- do not take more than directed (see overdose warning)
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adults |
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under 18 years of age |
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Inactive ingredients
Principal Display Panel
meijer®
Compare to Tylenol® 8HR Arthritis Pain active ingredient
PACKAGE NOT CHILD-RESISTANT
EASY OPEN CAP
8 HOUR arthritis pain relief
Acetaminophen
Extended-Release Tablets, 650 mg
Pain Reliever | Fever Reducer
For the Temporary Relief of Minor Arthritis Pain
DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN
150 Caplets* 650 mg each
*Capsule-Shaped Tablets
INGREDIENTS AND APPEARANCE
| ARTHRITIS PAIN RELIEF
acetaminophen tablet, film coated, extended release |
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| Labeler - Meijer Distribution Inc (006959555) |