Active Ingredient
Dimethicone 1%
Lucky
FDA Label NDC 20276-044
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Delta Brands Inc for the product Lucky (NDC 20276-044). 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, uses, warnings, when using this product, stop use and ask a doctor if, do not use on, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin protectant
Uses
■Helps prevent and temporarily protects chafed, chapped, or cracked skin
■Helps prevent and 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
■Condition worsens
■Symptoms last more than 7 days or clear up and occur again within a few days.
Do Not Use On
■Deep or puncture wounds
■Animal bites
■Serious burns
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Apply as needed
Inactive Ingredients
avena sativa (oat) kernel flour, benzyl alcohol, carbomer, ceteareth-20, cetrimonium chloride, cetearyl alcohol, FD&C blue no.1, FD&C yellow no.5, FD&C yellow no.6, glycerin, methylchloroisothiazolinone, methylisothiazolinone, mineral oil, petrolatum, p glycol, triethanolamine, tocopheryl acetate, water
Product Label
Product Label (Lckymstrzrdmth)
* Please review the disclaimer below.
