Extra Strength Pain Aid Tablet
Product Images NDC 69732-006

16 FDA label images from Hi-tech Nutaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Extra Strength Pain Aid (NDC 69732-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hi-tech Nutaceuticals, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Actives (Actives)

Actives (Actives)
A drug facts panel listing active ingredients in each tablet of Extra Strength Pain Aid: Acetaminophen 250 mg, Aspirin 250 mg (NSAID), and Caffeine 65 mg, each indicated as pain relievers with Aspirin also noted as a nonsteroidal anti-inflammatory drug.*
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Ask A Doc Or Pharm (Ask A Doc Or Pharm)

Ask A Doc Or Pharm (Ask A Doc Or Pharm)
A drug facts text panel advising consumers to ask a doctor or pharmacist before use if they have diabetes, gout, arthritis, or are using any other drug or under a doctor’s care for any serious condition.*
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Ask A Doc (Ask A Doc)

Ask A Doc (Ask A Doc)
A warning section from a drug facts label advising users to ask a doctor before use if they have liver disease, a history of stomach problems, high blood pressure, heart disease, liver cirrhosis, kidney disease, are taking a diuretic, or have asthma.*
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Keep Out Of Reach (Children)

Keep Out Of Reach (Children)
A drug facts panel warning section advising to keep the medication out of reach of children and to seek medical help or contact a Poison Control Center in case of overdose. It emphasizes the urgency of medical attention for both adults and children if any signs or symptoms occur.*
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Directions (Directions)

Directions (Directions)
A directions panel for Extra Strength Pain Aid tablets outlining dosage instructions. It advises against exceeding the recommended dose, instructs to drink a full glass of water with each dose, and specifies that adults and children 12 years and older should take 2 tablets every 6 hours with a maximum of 8 tablets in 24 hours. It also notes that children under 12 years should consult a doctor.*
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Do Not Use (Do Not Use)

Do Not Use (Do Not Use)
A drug facts panel excerpt from Extra Strength Pain Aid containing warnings about allergic reactions to acetaminophen, aspirin, or other pain relievers/fever reducers. It advises consulting a doctor or pharmacist if unsure about drug ingredients.*
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Inactives (Inactives)

Inactives (Inactives)
This image shows the inactive ingredients section of a drug facts label listing microcrystalline cellulose, dicalcium phosphate, sodium starch glycolate, magnesium stearate, stearic acid, and silica.*
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Pdp (Pdp)

Pdp (Pdp)
Label for Extra Strength Pain Aid tablets includes active ingredients Acetaminophen, Aspirin (NSAID), and Caffeine. The label features a red box with the product name in white letters and indicates package contains 30 tablets. The label also shows the Ameripharm Certified GMP Manufacturer logo and a comparison statement to Excedrin Extra Strength active ingredients.*
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Pregnant (Pregnant)

Pregnant (Pregnant)
A drug facts text panel warning about the use of aspirin during pregnancy or breastfeeding, advising consultation with a healthcare professional before use, especially avoiding aspirin in the last 3 months of pregnancy to prevent harm to the unborn child or delivery complications.*
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Questions (Questions)

Questions (Questions)
A drug facts or contact information panel showing a customer service phone number for questions or comments: 1.800.222.1888.*
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Stop Use (Stop Use)

Stop Use (Stop Use)
A drug facts panel section listing warnings to stop use and seek medical advice if allergic reactions or stomach bleeding symptoms occur, including fainting, vomiting blood, bloody stools, persistent stomach pain, ringing in ears, painful areas, worsening fever, or new symptoms. It advises consulting a doctor for these conditions.*
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Storage (Store)

Storage (Store)
The image shows a section titled 'Other information' with storage instructions including to store the product at 20°-25°C (68°-77°F), to close the cap tightly after use, to read all product information before use, and a warning not to use the product if the printed seal under the cap is cut, torn, or missing.*
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Indications (Uses)

Indications (Uses)
A drug facts panel section labeled 'Uses' listing conditions the medication temporarily relieves. These include minor aches and pains from headache, toothache, cold, arthritis, muscular aches, and premenstrual and menstrual cramps.*
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Warnings (Warnings)

Warnings (Warnings)
Warning text panel for Extra Strength Pain Aid tablets containing acetaminophen, aspirin, and caffeine. The panel includes warnings about Reye's syndrome, acetaminophen and aspirin allergy alerts, liver warnings, and stomach bleeding warnings related to NSAID use. It advises caution in children, elderly, and those with certain medical conditions.*
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More Warnings (Warnings2)

More Warnings (Warnings2)
A text panel containing a caffeine warning. It advises that the recommended dose contains about as much caffeine as a cup of coffee and warns to limit use of caffeine-containing medications, foods, or beverages while taking the product. It lists possible side effects of too much caffeine including nervousness, irritability, sleeplessness, and occasionally rapid heart beat.*
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When Using (When Using)

When Using (When Using)
This image shows a portion of a drug facts or warning text panel indicating a caution to consult a doctor if changes in behavior with nausea and vomiting occur, as these could be early signs of Reye's syndrome, a rare but serious illness. The text is part of the safety information commonly found on over-the-counter medication labels.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.