Saridon - A
FDA Label NDC 72689-0002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Oasis Trading for the product Saridon - A (NDC 72689-0002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

relief of: Headaches, Aches, Pain and Fever

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

■ adult and children 12 years of age and older: 1 capsules three times a day

■ children under 12 years of age: ask a doctor

Warnings

Do not use if carton is open or if printed bottle neck band or inner foil seal is broken.physician

Keep out of the reach of children. This package contains enough drug to seriously harm a child. Do not use with other drugs containing acetaminophen.

Use the smallest effective dose. Do not take more than the maximum daily dose. Overdose may result in severe or possibly fatal liver damage.

Do not take if allergic to acetaminophen. Consult a doctor if: your symptoms last for more than 5 days or fever lasts more than 3 days or you develop allergic reactions such as wheezing, rash or itching.

Ask a doctor or pharmacist before use if you: Are pregnant or breastfeeding, have chronic alcoholism; have a serious liver or kidney disease; use any other medications including natural health products, prescription drugs, salicylates or other pain and fever relief medications.

In case of overdose, call a Poison Control Centre or doctor immediately, even if you do not notice any possible signs or symptoms such as increased sweating, nausea, vomiting, stomach pain, and loss of appetite.

Inactive Ingredient

cellulose, corn starch, magnesium stearate, sodium starch glycolate

Dosage & Administration

For oral use only

Package Label.Principal Display Panel

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