![]() ![]() Keep out of reach of children/Accidental overdose warningsĭirection - dosage and when, how, or how often to take Stop use and ask a doctor if - signs of toxicity and other serious reactions that would require consumers to stop using the product immediately When using this product - side effects that could occur and substances or activities to avoid It will also require the information to appear in a standardized order, described below: Drug Facts - titleĪctive ingredient(s) - including amount in each dosage unitĭo not use - absolute contraindications, when the product should not be used under any circumstancesĪsk a doctor before use if you have - warnings for persons with certain preexisting conditions and for persons experiencing certain symptomsĪsk a doctor or pharmacist before use if you are - drug/drug and drug/food interactions For example, the new label will refer to uses instead of indications, and it will no longer use the terms precautions or contraindications. The new format will have standardized headings and subheadings using terms that will be more familiar to consumers. Specifically, in simple terms what will the new format look like?. ![]() It will also make it easier to compare similar products to determine which ingredients are right for them based on their symptoms and personal health situation. The new format will enable consumers to more readily and easily determine whether a product contains ingredients that they need or do not need or should not take. It will also help ensure that consumers select the right product to meet their needs. This action also will make it easier for consumers to understand information about products, benefits and risks and how the drugs should be used most effectively. FDA has finalized its regulation that will require nonprescription drugs to carry clear, simple and readable labeling.
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