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NDC 70677-0093-01 sunmark pain reliever 500 mg/1 Details
sunmark pain reliever 500 mg/1
sunmark pain reliever is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Strategic Sourcing Services LLC. 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: 70677-0093-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Acetaminophen
Product Information
| NDC | 70677-0093 |
|---|---|
| Product ID | 70677-0093_1e668f75-d4cd-4098-8e2b-0f44b30bbe85 |
| Associated GPIs | |
| GCN Sequence Number | 004490 |
| GCN Sequence Number Description | acetaminophen TABLET 500 MG ORAL |
| HIC3 | H3E |
| HIC3 Description | ANALGESIC/ANTIPYRETICS,NON-SALICYLATE |
| GCN | 16965 |
| HICL Sequence Number | 001866 |
| HICL Sequence Number Description | ACETAMINOPHEN |
| Brand/Generic | Generic |
| Proprietary Name | sunmark pain reliever |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | acetaminophen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | ACETAMINOPHEN |
| Labeler Name | Strategic Sourcing Services LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 70677-0093-01 (70677009301)
| NDC Package Code | 70677-0093-1 |
|---|---|
| Billing NDC | 70677009301 |
| Package | 1 BOTTLE in 1 CARTON (70677-0093-1) / 50 TABLET, FILM COATED in 1 BOTTLE |
| Marketing Start Date | 2020-01-22 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 1e668f75-d4cd-4098-8e2b-0f44b30bbe85 Details
Uses
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
- •
- more than 4,000 mg of acetaminophen in 24 hours
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- 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 have ever had an allergic reaction to this product or any of its ingredients
Keep out of reach of children.
Directions
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- do not take more than directed (see overdose warning)
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adults and children 12 years and over |
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Children under 12 years |
ask a doctor |
Inactive ingredients
Package/Label Principal Display Panel
INGREDIENTS AND APPEARANCE
| SUNMARK PAIN RELIEVER
acetaminophen tablet, film coated |
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| Labeler - Strategic Sourcing Services LLC (116956644) |