Active Ingredients
Avobenzone 3%
Homosalate 10%
Octisalate 5%
Petrolatum 40.2%
Jack Black Ointment
FDA Label NDC 66738-781
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jack Black L.l.c. for the product Jack Black (NDC 66738-781). 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, purposes, use, warning, otc - keep out of reach of children, directions, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purposes
Sunscreen
Sunscreen
Sunscreen
Skin protectant
Use
• Helps protect against sunburn and chapped lips.
Warning
Stop use if skin rash occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
• Apply liberally before sun exposure and reapply every 2 hours.
Inactive Ingredients
Beeswax, Ozokerite, Polyglyceryl-3 Beeswax, Butyloctyl Salicylate, Polypinene, Ethylhexyl Methoxycrylene, Hydrogenated Soybean Oil, Hydrogenated Coconut Oil, Fragrance, Theobroma Cacao (Cocoa) Seed Butter, Synthetic Beeswax, Cetyl Alcohol, Euphorbia Cerifera (Candelilla) Wax, Butyrospermum Parkii (Shea) Butter, Persea Gratissima (Avocado) Oil, Tocopheryl Acetate, Lecithin, Helianthus Annuus (Sunflower) Seed Oil, Microcrystalline Wax, Camellia Sinensis Leaf Extract
Questions?
1-469-341-2700; 1-877-766-3388 www.getJackBlack.com
* Please review the disclaimer below.
