Renewal
FDA Label NDC 11822-3351

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid for the product Renewal (NDC 11822-3351). 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 active ingredients, uses and directions, warnings, when using this product, stop using this product and ask a doctor if, keep out of reach of children, questions/comments?, package front and back labels (14oz), and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

  • MENTHOL 0.5% (TOPICAL ANALGESIC)
  • DIMETHICONE 5.0% (SKIN PROTECTANT)

Uses And Directions

  • USES: TO HELP MOISTURIZE, RELIEVE AND PROTECT DRY/ITCHY SKIN. RECOMMENDED FOR REPEATED USE.
  • DIRECTIONS: APPLY TO DRY, ITCHY SKIN AS OFTEN AS NEEDED

Warnings

  • FOR EXTERNAL USE ONLY.

When Using This Product

  • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

Stop Using This Product And Ask A Doctor If

  • IRRITATION OR REDNESS DEVELOPS AND LASTS.

Keep Out Of Reach Of Children

  • IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Questions/Comments?

1-866-695-3030

Package Front And Back Labels (14Oz)

  • 14OZ FRONT AND BACK LABELS: ra14.jpg
    Front And Back Labels (Ra14)

    Front And Back Labels (Ra14)

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