Active Ingredient
Dimethicone, Butyl Methoxydibenzoylmethane, Titanium Dioxide, Octyl Methoxycinnamate.
Iqqu Advance Sunscreen
FDA Label NDC 50403-999
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Iqqu Usa Co. for the product Iqqu Advance Sunscreen (NDC 50403-999). 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, directions, warnings, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions
Advance formula, use a small amount only. Apply evenly over clean skin until fully absorbed. Apply as needed before sun exposure.
Keep the sunscreen tube away from direct sunlight to preserve its efficiency.
Warnings
For external use only. Avoid contact with the eyes. Discontinue use if signs of irritation occurs. Keep out of children’s reach.
Inactive Ingredients
Isononyl Isonanonate, Glyceryl Stearate, Cyclopentasiloxane (and) Dimethicone, Cyclopentasiloxane (and) C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Talcum
Manufactured by: June Laboratories Co., Ltd.
1014 Soi Wat Channai, Sathupradit Rd,
Bangkok 10120 Thailand.
Made in Thailand
www.iqqubeauty.com
Principal Display Panel
Package Label – 30 mL
IQQU Advance Sunscreen
SPF 35 UVA/UVB
30 mL /1.01 oz
Principal Display Panel (30 mL /1.01 oz)
* Please review the disclaimer below.
