Revlon Youth FX

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Revlon Youth FX
Generic name
ZINC OXIDE, TITANIUM DIOXIDE MAKE-UP
Manufacturer
Revlon Consumer Products Corp
Product type
HUMAN OTC DRUG
SPL set ID
442dec1e-032c-28de-e054-00144ff8d46c
SPL ID
2a96c7e3-ff5a-553e-e063-6294a90a2fd7
Version
3
Effective date
2024-12-31
Source export date
2026-10-27
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:59:51
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

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 a rash occurs Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control center right away Directions: Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hours Children under 6 months: Ask a doctor. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 am - 2 pm Wear long-sleeved shirts, pants, hats and sunglasses.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.