84417-002

Manufacturer
Fitish Holdings, LLC | Guangdong Aimu Biological Technology Co., Ltd
Effective date
2026-07-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-07-18 05:11:10

Label at a glance#

ProductFITISH SPF 50 FACE
Active ingredientOCTINOXATE, OCTOCRYLENE, OCTISALATE
Label structure12 sections

Dosage and administration

Apply directly to clean skin 15 minutes before sun exposure and anywhere you want extra glow. Reapply after 40 minutes of swimming or sweating, immediately after towel drying and at least every 2 hours. Can be used on body as well. 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 valu...

Storage and handling

No data available

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 8.0% Ethylhexyl Salicylate 5.0% Ethylhexyl Methoxycinnamate 7.5 %

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

USES Helps prevent sunburn

Warnings

WARNINGS SECTION

WARNINGS For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask doctorif rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply directly to clean skin 15 minutes before sun exposure and anywhere you want extra glow. Reapply after

40 minutes of swimming or sweating, immediately after towel drying and at least every 2 hours. Can be used

on body as well.

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 limiting time in the sun, especially from 10 a.m.-2 p.m. and wear long-sleeved

shirts, pants, hats and sunglasses


Other information

STORAGE AND HANDLING SECTION

No data available

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Yohjyu Matsu Ekisu (Aloe Vera), C12-15 Alkyl Benzoate, Camellia Sinensis Leaf Extract, Camellia Sinensis Leaf Oil, Caprylic/Capric Triglyceride, Cetyl Ethylhexanoate, Cocos Nucifera
(Coconut) Oil, Cocos Nucifera Extract, Cyclopentasiloxane, Dextrin Palmitate, Dibutyl Ethylhexanoyl Glutamide, Dibutyl Lauroyl Glutamide, Dicaprylyl Carbonate, Ethyl Macadamiate, Ethylhexyl
Isopalmitate, Isononyl Isononanoate, Isopropyl Lauroyl Sarcosinate, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopherol (Vitamin E)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84417-00284417-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-08-15full-release2026-06-01 00:17:18

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FITISH SPF 50 FACEFITISH SPF 50 FACEFitish Holdings, LLC1c44a572-59e6-c3c5-e063-6394a90a0e242026-07-14WarningsExact identifier
ndc (package): 84417-002-01
ndc (product): 84417-002
ndc11 (package): 84417000201
spl id: 569ce846-37d3-9a7d-e063-6394a90a6309
spl set id: 1c44a572-59e6-c3c5-e063-6394a90a0e24

Reported adverse events (FAERS/openFDA)#

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