Otc - Active Ingredient
Active Ingredients: Octinoxate 7%, Oxybenzone 3%
Bubble Gum Sunscreen Lip Moisturizer
FDA Label NDC 75866-301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Beacon Promotions for the product Bubble Gum Sunscreen Lip Moisturizer (NDC 75866-301). 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, dosage & administration, storage and handling, inactive ingredient, other, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications & Usage
Use: helps prevent sunburn
Warnings
Warning: stop use if skin rash occurs
Dosage & Administration
Directions: Apply and reapply at least every 2 hours for sunburn protection. children under 6 months of age: ask a doctor.
Storage And Handling
Other information: Store at 68-77F (20-25C)
Inactive Ingredient
Inactive Ingredients:
Mineral Oil, Polybutene, Ethylhexyl Palmitate, Parafin, Ceresin, Microcrystalline Wax, Petrolatum, Beeswax, Fragrance, Methylparaben, Propylparaben, BHT.
Other
HC301LB Dist. by Beacon Promotions Inc.
New lm, MN 56073
(507) 233-3278
Made in China
Package Label.Principal Display Panel
Sunscreen Bubble Bum (Bubblegumbalm)
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