Nerve Tonic Tablet
FDA Label NDC 54973-3014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hyland's Inc. for the product Nerve Tonic (NDC 54973-3014). 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 other, otc - active ingredient, otc - purpose, uses, otc - ask doctor, otc - keep out of reach of children, otc - do not use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

In case of emergency, contact a medical professional or poison control center immediately. Hyland's may also be contacted for emergency information about our products 24 hours a day, 7 days per week at (800) 624-9659.

Uses

Temporarily relieves the symptoms of stress, nervousness, mental anxiousness, irritability, and the inability to concentrate.

Otc - Ask Doctor

As with any drug, ask a doctor before use if pregnant or nursing. Consult a physician if:

  • Symptoms persist for more than 7 days or worsen

Otc - Keep Out Of Reach Of Children

Keep this and all medications out of the reach of children. In case of accidental overdose, contact a medical professional or a poison control center immediately.

Otc - Do Not Use

Do not use if imprinted tamper band is broken or missing.

Directions

Adults & children 12 years and over: Dissolve 1-2 tablets under tongue 3 times per day. Children 6 years to under 12 years: Dissolve 1 tablet under tongue 3 times per day. Sudden onset: Every 15 minutes for up to 6 doses.

Questions Or Comments?

(800) 624-9659

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