Wknd Underwater Sun White
FDA Label NDC 71192-030

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Surfcode for the product Wknd Underwater Sun White (NDC 71192-030). 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, inactive ingredient, purpose, warnings, description, 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

Active Ingredient

Active ingredients: Titanium Dioxide 24.25%, Octocrylene 10.00%, Homosalate 10.00%, Ethylhexyl Salicylate 5.00%, Butyl Methoxydibenzoylmethane 3.00%

Inactive Ingredient

Inactive Ingredients: Isopropyl Myristate, Triethyl Citrate, Ceresin, Talc, Methyl Methacrylate Crosspolymer, Euphorbia Cerifera (Candelilla) Wax, Cetyl Ethyhexanoate, Microcrystalline Wax, Polyethylene, Beeswax, Bis-EthylHexylOxyphenol Methoxyphenyl Triazine, Dimethicone, Silica Dimethyl Silylate, Phenoxyethanol

Purpose

Purpose: Sunscreen

Warnings

WARNINGS :

FOR EXTERNAL USE ONLY

Do not use on damaged or broken skin

When using this product, Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

Description

USES:

- Help prevent sunburn

- Higher SPF gives more sunburn protection

- Retains SPF after 180 minutes of activity in the water or sweating

DIRECTION: Apply liberally and uniformly to all exposed areas before sun exposure.

* Please review the disclaimer below.