Nervive Pain Relieving Spray
FDA Label NDC 84126-319

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Nervive Pain Relieving (NDC 84126-319). 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, active ingredients, active ingredients purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

When Using This Product

  • use only as directed. Read and follow all directions and warnings on this label.
  • avoid contact with eyes and mucous membranes.
  • do not spray in face or mouth
  • rare cases of serious burns have been reported with products of this type
  • do not apply to wounds or damaged, broken, blistered or irritated skin
  • do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use
  • a transient burning sensation may occur upon application but generally disappears in several days
  • avoid applying into skin folds

Overdosage

If swallowed, get medical help or contact a Poison Control Center right away.

* Please review the disclaimer below.