Rexall
FDA Label NDC 55910-316

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dolgencorp Inc for the product Rexall (NDC 55910-316). 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 ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, do not use on, keep out of reach of chidren, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

PETROLATUM 99.8%

Purpose

SKIN PROTECTANT

Use

  • TEMPORARILY PROTECTS MINOR:
  • CUTS
  • SCRAPES
  • BURNS
  • TEMPORARILY PROTECTS AND HELPS RELIEVE CHAPPED OR CRACKED SKIN AND LIPS
  • HELPS PROTECT FROM THE DRYING EFFECTS OF WIND AND COLD WEATHER

Warnings

FOR EXTERNAL USE ONLY

When Using This Product

DO NOT GET INTO EYES

Stop Use And Ask A Doctor If

CONDITIONS LASTS MORE THAN 7 DAYS

Do Not Use On

  • DEEP PUNCTURE WOUNDS
  • ANIMAL BITES
  • SERIOUS BURNS

Keep Out Of Reach Of Chidren

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY

Directions

APPLY AS NEEDED

Inactive Ingredients

ALOE BARBADENSIS LEAF JUICE, FRAGRANCE (PARFUM), TOCOPHERYL ACETATE

Label Copy

Image Of The Label (20130l)

Image Of The Label (20130l)

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