RIGHT REMEDIES EXTRA STRENGTH Pain Relief PM Caplet

Manufacturer
Strive Pharmaceuticals Inc.
Effective date
2026-06-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-07-17 21:37:10

Label at a glance#

ProductRIGHT REMEDIES EXTRA STRENGTH Pain Relief PM Caplet
Active ingredientACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE
Label structure10 sections

Indications and uses

• Temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness

Dosage and administration

•  do not take more than directed (see overdose warning) ​  adults and children 12 years and over • take 2 caplets at bedtime • do not take more than 2 caplets of this product in 24 hours  children under 12 years do not use

Storage and handling

• store at room temperature between 20°-25°C (68°-77°F) • protect from light, heat and moisture

Label contents#

Full prescribing information#

Active ingredients (in each caplet)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 500 mg
Diphenhydramine HCl 25 mg

Purpose

OTC - PURPOSE SECTION

Pain reliever
Nighttime sleep aid

Uses

INDICATIONS & USAGE SECTION

• Temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness

Warnings

WARNINGS SECTION

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.
• with any other product containing diphenhydramine, even one used on skin • in children under 12 years of age
• 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 • a breathing problem such as emphysema or chronic bronchitis • trouble urinating due to an enlarged prostate gland • glaucoma

Ask a doctor or pharmacist before use if you are
• taking the blood thinning drug warfarin • taking sedatives or tranquilizers

When using this product
• drowsiness will occur • avoid alcoholic drinks
• do not drive a motor vehicle or operate machinery

Stop 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 lasts more than 10 days
• fever gets worse or lasts more than 3 days • redness or swelling is present • new symptoms occur.
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.
Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

• do not take more than directed (see overdose warning)​

 adults and children 12 years and over• take 2 caplets at bedtime
• do not take more than 2 caplets of this product in 24 hours
 children under 12 yearsdo not use

Other information

STORAGE AND HANDLING SECTION

• store at room temperature between 20°-25°C (68°-77°F) • protect from light, heat and moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C Blue No. 1, FD&C Blue No. 2, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, polyvinylpyrrolidone, pregelatinized starch, stearic acid powder, titanium dioxide

Questions or comments?

OTC - QUESTIONS SECTION

1-888-577-8033 Monday - Friday 8am - 4pm EST

SPL UNCLASSIFIED SECTION

Compare to the active ingredients in Extra Strength Tylenol® PM*

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

*This product is not manufactured or distributed by Kenvue, Inc., owner of the registered trademark Tylenol®​.

​Distributed by:

Strive Pharmaceuticals Inc.
East Brunswick, NJ 08816

PRODUCT OF INDIA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RR EXTRA STRENGTH Pain Relief PM CapletRR EXTRA STRENGTH Pain Relief PM Caplet

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130370692000450GTIN-13: 0370692000450
EAN-13: 0370692000450
GTIN-12: 370692000450
UPC-A: 370692000450
GTIN storage (14 digits): 00370692000450
70692471-2.jpg
QR code linkQR Codewww.strivepharma.com/70692471-2.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
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Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70692-47170692-471-31, 70692-471-84

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-03-17full-release2026-06-01 00:57:26

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RIGHT REMEDIES EXTRA STRENGTH Pain Relief PM CapletACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDEStrive Pharmaceuticals Inc.2d63671d-cf7c-bbdd-e063-6294a90affef2026-06-15WarningsExact identifier
ndc (package): 70692-471-31
ndc (package): 70692-471-84
ndc (product): 70692-471
ndc11 (package): 70692047131
ndc11 (package): 70692047184
spl id: 28e68866-abb6-4870-96ad-9b062ce40f8a
spl set id: 2d63671d-cf7c-bbdd-e063-6294a90affef

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.