Head And Cold Tablet
Product Images NDC 69732-003

16 FDA label images from Hi-tech Nutraceuticals, 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 Head And Cold (NDC 69732-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hi-tech Nutraceuticals, 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.

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Ask Doc Or Pharm (Ask A Doc Or Pharm)

Ask Doc Or Pharm (Ask A Doc Or Pharm)
This text panel contains a warning advising users to consult a doctor or pharmacist before using the product if they are taking the blood thinning drug warfarin. The text emphasizes safety precautions related to drug interactions.*
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Ask A Doc (Ask A Doc)

Ask A Doc (Ask A Doc)
This drug facts or warning panel advises users to consult a doctor before use if they have liver disease, thyroid disease, heart disease, diabetes, high blood pressure, trouble urinating due to an enlarged prostate gland, persistent or chronic cough related to smoking, asthma, chronic bronchitis or emphysema, or a cough with excessive phlegm (mucus).*
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Dosage And Admin (Directions)

Dosage And Admin (Directions)
Directions panel for Head and Cold tablets showing dosage instructions for adults and children 12 years and over, including taking 2 caplets every 4 hours with swallowing whole, and not exceeding 12 caplets in 24 hours. It also cautions against use in children under 12 years due to overdose risk and potential liver damage.*
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Pdp (Pdp)

Pdp (Pdp)
The packaging label for Cold + Head Congestion Severe tablets features the brand name prominently in white text on a red background. It highlights acetaminophen, phenylephrine HCl, and guaifenesin as active ingredients, noting their roles as pain reliever, fever reducer, nasal decongestant, and expectorant. The label also states the product is for adults and contains 30 caplets. There is a logo for Ameripharm Certified GMP Manufacturer and a comparison to Tylenol Cold + Head active ingredients.*
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Questions (Questions)

Questions (Questions)
A text panel titled 'Questions or comments?' providing a customer service phone number: 1.717.667.2142 for inquiries related to the product.*
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Atop Use (Stop Use And Ask Doc)

Atop Use (Stop Use And Ask Doc)
A drug facts warning panel listing conditions to stop use and consult a doctor, including nervousness, dizziness, sleeplessness, worsening or prolonged pain, nasal congestion, cough, fever, redness or swelling, new symptoms, and cough with rash or prolonged headache, as possible signs of a serious condition.*
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When Using (When Using)

When Using (When Using)
A single-line text panel with a safety warning stating, "When using this product do not exceed recommended dosage." This advice is typically found on medication labeling to caution users against overuse.*
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Actives (Active And Purp)

Actives (Active And Purp)
Drug Facts panel listing active ingredients and their purposes in each caplet of Head and Cold tablets by Hi-Tech Nutraceuticals, LLC. Ingredients include Acetaminophen 325 mg (pain reliever), Guaifenesin 200 mg (expectorant), Dextromethorphan HBr 10 mg (cough suppressant), and Phenylephrine HCl 5 mg (nasal decongestant).*
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Do Not Use (Do Not Use)

Do Not Use (Do Not Use)
This panel contains warnings under the heading 'Do not use' for the Head and Cold tablet. It advises against use with other products containing acetaminophen, concurrent use with monoamine oxidase inhibitors (MAOI) or within two weeks of stopping such drugs, and if there has been an allergic reaction to the product or its ingredients.*
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Inactives (Inactive)

Inactives (Inactive)
Text panel listing inactive ingredients of Head and Cold tablets, including microcrystalline cellulose, dicalsium phosphate, sodium starch glycolate, magnesium stearate, stearic acid, and silica.*
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Overdosage (Overdose)

Overdosage (Overdose)
A drug facts or safety information panel displaying an overdose warning for Head and Cold tablets. It advises getting medical help or contacting a Poison Control Center immediately at 1-800-222-1222 in case of overdose and emphasizes the importance of quick medical attention for both adults and children regardless of observed symptoms.*
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Pregnant (Pregnant)

Pregnant (Pregnant)
A warning statement advising that individuals who are pregnant or breastfeeding should consult a healthcare professional before using the product.*
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Keep Out Of Reach (Reach)

Keep Out Of Reach (Reach)
A drug facts text panel containing warnings for the product Head and Cold, including an advisory to keep the product out of reach of children. The text is part of the medication's safety information.*
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Storage (Store)

Storage (Store)
A drug facts or information panel displaying storage instructions for the medication. It states to store the product between 20-25°C (68-77°F) and warns not to use if the printed seal under the cap is cut, torn, or missing.*
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Uses (Uses)

Uses (Uses)
A text panel listing the uses of the drug, including relief of minor aches and pains, headache, sore throat, nasal congestion, sinus congestion and pressure, cough, and helping to loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.*
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Warnings (Warnings)

Warnings (Warnings)
Warning panel from Head and Cold tablet label containing acetaminophen, guaifenesin, dextromethorphan HBr, and phenylephrine HCl. The warnings include a liver warning about acetaminophen-related severe liver damage risks and a sore throat warning advising consultation with a doctor if symptoms worsen or persist more than 2 days.*

* 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.