Lypsyl Honeyberry
FDA Label NDC 62721-8106

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Lornamead for the product Lypsyl Honeyberry (NDC 62721-8106). 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, use, warnings, otc - keep out of reach of children, directions, questions or comments, inactive ingredients, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Octyl Methoxycinnamate 5.5%...............SunscreenOctocrylene 2.0%..................................SunscreenOxybenzone 3.5%.................................Sunscreen

Use

Helps prevent sunburn

Warnings

Stop use and ask a doctor - if rash or irritation develops and lasts

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control

Center right away.

Directions

Apply Liberally before sun exposure and as needed - children under 6 months of age: ask a doctor

Inactive Ingredients

Beeswax, Persea Gratissima (Avocado)Butter, Butyrospermum Parkii (Shea Butter), SimmondsiaChinensis (Jojoba) Seed Oil, Flavor, Tocopheryl Acetate (Vitamin EAcetate), Retinyl Palmitate (Vitamin A Palmitate)

Dosage & Administration

Apply Liberally before sun exposure and as needed

* Please review the disclaimer below.