Indications and uses
• temporarily relieves minor aches and pains due to: • the common cold • headache • backache • minor pain of arthritis • toothache • muscular aches • premenstrual and menstrual cramps • temporarily reduces fever.
RIGHT REMEDIES Pain Relief Caplet
- Manufacturer
- Strive Pharmaceuticals Inc.
- Effective date
- 2022-07-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:50:29
Label at a glance#
ProductRIGHT REMEDIES Pain Relief Caplet
Active ingredientACETAMINOPHEN
Label structure10 sections
Dosage and administration
Do not take more than directed. SEE OVERDOSE WARNING . adults & children 12 years of age and over • take 2 caplets every 6 hours while symptoms last • do not take more than 6 caplets in 24 hours, unless directed by doctor • do not take more than 10 days, unless directed by a doctor children under 12 years of age • ask a doctor
Storage and handling
• store at room temperature between 20 - 25ºC (68-77ºF). • avoid excessive heat, cold and humidity. • close cap tightly after use. TAMPER EVIDENT: Do not use if imprinted safety seal is broken or missing.
Label contents#
Full prescribing information#
Active Ingredient (in each caplet)
Acetaminophen 500mg
Purpose
Pain reliever/fever reducer
Uses
• temporarily relieves minor aches and pains due to:
• the common cold • headache
• backache • minor pain of arthritis
• toothache • muscular aches
• premenstrual and menstrual cramps
• temporarily reduces fever.
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
• 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.
• if you have ever had an allergic reaction to this product or any of its ingredients.
Ask a doctor before use if you have liver disease
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
Stop use and ask a doctor if • pain gets worse or lasts more than 10 days • fever gets worse or lasts more than 3 days • new symptoms occur • redness or swelling is present. These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. OVERDOSE WARNING: In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.
Directions
Do not take more than directed. SEE OVERDOSE WARNING.
| adults & children 12 years of age and over | • take 2 caplets every 6 hours while symptoms last • do not take more than 6 caplets in 24 hours, unless directed by doctor • do not take more than 10 days, unless directed by a doctor |
| children under 12 years of age | • ask a doctor |
Other information
• store at room temperature between 20 - 25ºC (68-77ºF).
• avoid excessive heat, cold and humidity.
• close cap tightly after use.
TAMPER EVIDENT: Do not use if imprinted safety seal is broken or missing.
Inactive ingredients
hydroxypropyl methylcellulose, maltodextrin, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate, starch, stearic acid
Questions or comments?
Call 1 (888) 577 - 8033
SPL UNCLASSIFIED SECTION
†compare to active ingredient in TYLENOL ® Extra Strength Caplets
EXTRA STRENGTH
Distributed by: STRIVE PHARMACEUTICALS INC.
East Brunswick, NJ 08816
READ AND KEEP OUTER PACKAGE FOR COMPLETE PRODUCT INFORMATION
†This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division., owner of the registered trademark Tylenol® Extra Strength Caplets.
Packaging
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70692-141-42 | 2024-01-30 | C162847 | 48780-1 | 1030e364-fa3b-111a-e063-dadaa90a10e2 | RIGHT REMEDIES Pain Relief Caplet |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70692-141-42 | RIGHT REMEDIES Pain Relief Caplet | 24 in 1 PACKAGE | TABLET, COATED | 24 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- RIGHT REMEDIES Pain Relief Caplet
- Acetaminophen
- HYPROMELLOSE, UNSPECIFIED
- MALTODEXTRIN
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- SODIUM STARCH GLYCOLATE TYPE A
- STARCH, CORN
- STEARIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70692-141 | 70692-141-42 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| POVIDONE, UNSPECIFIED | FZ989GH94E | IACT |
| SODIUM STARCH GLYCOLATE TYPE A | H8AV0SQX4D | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| a400cd15-5a12-4aec-ba98-b7a670ea571b | 44f7626c-0f9a-4eba-956b-14eeedcdc444 | 2022-07-20 | Warnings | a400cd15-5a12-4aec-ba98-b7a670ea571b 44f7626c-0f9a-4eba-956b-14eeedcdc444 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.