Daily Moisturizing Lotion
FDA Label NDC 41250-619
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Meijer, Inc. for the product Daily Moisturizing (NDC 41250-619). 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 otc - active ingredient, indications & usage, warnings, otc - when using, otc - stop use, storage and handling, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications & Usage
Uses helps prevent and temporarily protects chafed, chapped, cracked or windburned skin.
Warnings
Otc - When Using
Otc - Stop Use
Stop use and ask a doctor if condition worsens or does not improve within seven days
Storage And Handling
Keep out or reach of children. If swallowed, get medical help or contract a Poison Control Center right away
Dosage & Administration
Directions apply liberally as often as necessary
Inactive Ingredient
Inactive ingredients allantoin, Avena sativa (oat) kernel flour, benzyl alcohol, cety alcohol, distearyldimonium chloride, glycerin, isopropyl palmitate, petrolatum, sodium chloride, water
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