TULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30

Manufacturer
PML NYC, LLC
Effective date
2026-04-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:54:05

Label at a glance#

ProductTULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30
Active ingredientAVOBENZONE, OCTISALATE
Label structure10 sections

Indications and uses

Helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

Apply liberally 15 minutes before sun exposure. 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 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. Children under 6 mo...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Octisalate 5%

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

USES

OTC - WHEN USING SECTION

Helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

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.

Keep out of reach of children

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 liberally 15 minutes before sun exposure. 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 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. Children under 6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, C9-12 Alkane , Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Ethylhexyl Palmitate, Triethylhexanoin, Polyglyceryl-6 Polyhydroxystearate, Polyglyceryl-6 Polyricinoleate, Isododecane, Silica, Butylene Glycol, Disteardimonium Hectorite, Trimethylsiloxysilicate, VP/Eicosene Copolymer, Glycerin, Argania Spinosa Kernel Oil, Tocopheryl Acetate, VP/Hexadecene Copolymer, Octyldodecyl Neopentanoate, Sodium Chloride, Magnesium Sulfate, Boron Nitride, Sorbitan Oleate, Polyglycerin-6, Caesalpinia Spinosa Fruit Extract, Octyldodecanol, Safflower oil/ Palm oil aminopropanediol esters , Mica , Lactococcus Ferment Lysate, Alpha-Glucan Oligosaccharide, Hydrogenated Lecithin, Bisabolol, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Simethicone, Kappaphycus Alvarezii Extract, Pongamia Glabra Seed Oil , Beta Vulgaris (Beet) Root Extract, Cystoseira Tamariscifolia Extract, Inulin, Niacinamide, Tocopherol, Tetrahexyldecyl Ascorbate, Ascorbyl Palmitate, Lactic Acid, Polymnia Sonchifolia Root Juice, Lactobacillus Ferment, Curcuma Longa (Turmeric) Root Extract, Maltodextrin, Ceramide NP, Dunaliella Salina Extract , Haematococcus Pluvialis Extract , Acacia Seyal Gum Extract, Lactobacillus, Ethylhexylglycerin, Aluminum Hydroxide, Sodium Hyaluronate, Citric Acid, 1,2-Hexanediol, Caprylyl Glycol, Phenoxyethanol, Sodium Benzoate, Potassium Sorbate, Titanium Dioxide (CI 77891), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499).

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if rash occurs.

RECENT MAJOR CHANGES SECTION

dosage & admin update

PRINCIPLE DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

innerinnerLabel-cartonLabel-carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59735-204-012026-01-29C16284748780-149896155-add7-586f-e063-e6dba90add90TULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59735-204-01TULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 301 in 1 CARTONLOTION13
59735-204-01TULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 3030 mL in 1 TUBELOTION303

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 66 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59735-20459735-204-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 64 matching rows.

Source Document#

Source XML

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30BRIGHTENING SKIN TINTPML NYC, LLCf4c0f2d9-3e2f-5358-e053-2995a90aeb842026-04-14WarningsExact identifier
ndc (package): 59735-204-01
ndc (product): 59735-204
ndc11 (package): 59735020401
spl id: 4f780111-20b6-c827-e063-6294a90a5d2a
spl set id: f4c0f2d9-3e2f-5358-e053-2995a90aeb84

Reported adverse events (FAERS/openFDA)#

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