Active Ingredient
DIMETHICONE 1.25%
Daily Moisturizing
FDA Label NDC 41163-320
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Supervalu Inc for the product Daily Moisturizing (NDC 41163-320). 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, warning, when using this product, stop using this product and ask a doctor if, keep out of reach of children, purpose, questions/comments?, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warning
FOR EXTERNAL USE ONLY.
When Using This Product
AVOID CONTACT WITH EYES, IF CONTACT OCCURS, RINSE EYE THROUGHLY WITH WATER.
Stop Using This Product And Ask A Doctor If
CONDITION WORSENS OR SYMPTOMS PERSIST FOR MORE THAN SEVEN DAYS OR OCCUR AGAIN WITHIN A FEW DAYS.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Purpose
SKIN PROTECTANT
Questions/Comments?
1 - 877 - 932 - 7948
Directions
ADULTS AND CHILDREN OVER 2 YEARS: APPLY AS NEEDED.
Uses
TEMPORARILY PROTECTS AND HELPS RELIEVE CHAPPED OR CRACKED SKIN.
Inactive Ingredients
WATER (AQUA), GLYCERIN, DISTEARYLDIMONIUM CHLORIDE, PETROLATUM, ISOPROPYL PALMITATE, CETYL ALCOHOL, AVENA SATIVA (OAT) KEMEL FLOUR, BENZYL ALCOHOL, SODIUM CHLORIDE, DMDM HYDANTOIN, METHYLPARABEN, PROPYLPARABEN
Package Front And Back Labels
12 OZ FRONT AND BACK LABELS: equaline12.jpg
12 Oz Front And Back Labels (Equaline12)
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