FDA.reportPublic FDA data

Quick Dry Body

Manufacturer
MDSolarSciences
Effective date
2025-06-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:02:24

Label at a glance#

ProductQuick Dry Body Broad Spectrum SPF40 Sunscreen UVA-UVB Sunscreen with SolSci-X
Active ingredientAVOBENZONE, OCTISALATE, OCTOCRYLENE
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 Spray on hands and rub well into face and scalp Reapply: After 80 minutes of swimming or sweating Immediately after towel drying 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 the risk, regularly use a sunscreen with Broad Spectrum SPF o...

Storage and handling

Protect the product in this container from excessive heat May stain some fabrics You may report serious adverse reactions to Report Reaction, LLC. PO Box 22, Plainsboro, NJ 08536-0222

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
Avobenzone 3%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 2.75%Sunscreen

Uses

INDICATIONS & USAGE 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

OTC - WHEN USING SECTION

When using this productavoid spraying in eyes. Rinse with water to remove.

OTC - DO NOT USE SECTION

Do not useon damaged or broken skin

OTC - STOP USE SECTION

Stop use and ask a doctorif rash or irritation develops and lasts.

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.

Flammable

SPL UNCLASSIFIED SECTION

Do not puncture or incinerate

Contents under pressure (compressed air)

Do not use near heat or flame or while smoking

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure
  • Spray on hands and rub well into face and scalp
  • Reapply:
    • After 80 minutes of swimming or sweating
    • Immediately after towel drying
    • 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 the risk, regularly use a sunscreen with Broad Spectrum SPF of 15 or higher and other sun protection measures including:
    • Limit time in the sun, especially from 10a.m. – 2p.m.
    • Wear long-sleeved shirts, pants, hats and sunglasses.

Other Information

STORAGE AND HANDLING SECTION

  • Protect the product in this container from excessive heat
  • May stain some fabrics
  • You may report serious adverse reactions to Report Reaction, LLC. PO Box 22, Plainsboro, NJ 08536-0222

Inactive ingredients

INACTIVE INGREDIENT SECTION

SD Alcohol 40, Butyloctyl Salicylate, Polyester-8, Caprylyl Methicone, Diisopropyl Adipate, Acrylates/Octylacrylamide Copolymer, Tetrahexlydecyl Ascorbate, EDTA, Phytic Acid, Phyllanthus Emblica Fruit Extract, Trisodium Ethylenediamine Disuccinate

SPL UNCLASSIFIED SECTION

Distributed by:
MDSolarSciences Corp.
40 Richards Avenue, 3rd Fl., Norwalk, CT 06854

PRINCIPAL DISPLAY PANEL - 148 mL Can Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MDSolar Sciences™

40
QUICK DRY
BODY
SPRAY
with SolSci-X ™

BROAD SPECTRUM
SPF 40
UVA-UVB SUNSCREEN

+R
enhanced with
ProVention-R ™

developed & approved
by Dermatologists

Water resistant (80 minutes)
Non-comedogenic – won't clog pores

sun care

Net Wt. 148 mL - 5 Fl. Oz.

PRINCIPAL DISPLAY PANEL - 148 mL Can Carton
PRINCIPAL DISPLAY PANEL - 148 mL Can Carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49358-556-012025-06-05C16284748780-1f386c64a-02a2-0266-e053-dadaa90a7c1aQuick Dry Body Spray 5Fl Oz Broad Spectrum SPF40 Sunscreen UVA-UVB Sunscreen with SolSci-X™
49358-556-012023-01-30C16284748780-1f386c64a-02a2-0266-e053-dadaa90a7c1aQuick Dry Body Spray 5Fl Oz Broad Spectrum SPF40 Sunscreen UVA-UVB Sunscreen with SolSci-X™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49358-556-01Quick Dry BodyBroad Spectrum SPF40 Sunscreen UVA-UVB Sunscreen with SolSci-X148 g in 1 CANSPRAY1483
49358-556-01Quick Dry BodyBroad Spectrum SPF40 Sunscreen UVA-UVB Sunscreen with SolSci-X1 in 1 CARTONSPRAY13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AvobenzoneACTIVE INGREDIENTG63QQF2NOX1
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
AvobenzoneACTIVE MOIETYG63QQF2NOX1
OctisalateACTIVE MOIETY4X49Y0596W1
OctocryleneACTIVE MOIETY5A68WGF6WM1
AlcoholINACTIVE INGREDIENT3K9958V90M1
Butyloctyl SalicylateINACTIVE INGREDIENT2EH13UN8D31
Caprylyl TrisiloxaneINACTIVE INGREDIENTQ95M2P1KJL1
Carbomer Copolymer Type A (Allyl Pentaerythritol Crosslinked)INACTIVE INGREDIENT71DD5V995L1
Diisopropyl AdipateINACTIVE INGREDIENTP7E6YFV72X1
Edetic AcidINACTIVE INGREDIENT9G34HU7RV01
Fytic AcidINACTIVE INGREDIENT7IGF0S7R8I1
Phyllanthus Emblica FruitINACTIVE INGREDIENTYLX4CW25761
Polyester-8 (1400 MW, Cyanodiphenylpropenoyl Capped)INACTIVE INGREDIENTT9296U138P1
Tetrahexyldecyl AscorbateINACTIVE INGREDIENT9LBV3F07AZ1
Trisodium Ethylenediamine DisuccinateINACTIVE INGREDIENTYA22H34H9Q1

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49358-55649358-556-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED)T9296U138PIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
EDETIC ACID9G34HU7RV0IACT
FYTIC ACID7IGF0S7R8IIACT
PHYLLANTHUS EMBLICA FRUITYLX4CW2576IACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
TRISODIUM ETHYLENEDIAMINE DISUCCINATEYA22H34H9QIACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 16 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Edetic AcidEDETIC ACID9G34HU7RV0SOLUTION / TOPICAL0.5 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SUSPENSION / TOPICAL0.06 %w/vExact identifier — unii+route
10 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SUSPENSION / TOPICAL0.06 %w/vExact identifier — unii+route
10 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0GEL / TOPICAL0.1 %w/wExact identifier — unii+route
10 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0CREAM / TOPICAL0.5 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0CREAM / TOPICAL0.5 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Carbomer Copolymer Type A (Allyl Pentaerythritol Crosslinked)CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LLOTION / TOPICAL21 mgExact identifier — unii+route
2 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0GEL / TOPICAL0.1 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Carbomer Copolymer Type A (Allyl Pentaerythritol Crosslinked)CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LLOTION / TOPICAL21 mgExact identifier — unii+route
2 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XSPRAY / TOPICAL360 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XSPRAY / TOPICAL360 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SOLUTION / TOPICAL0.5 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SHAMPOO / TOPICAL0.2 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SHAMPOO / TOPICAL0.2 %w/wExact identifier — unii+route
10 equally ranked IID candidates

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
Quick Dry Body Broad Spectrum SPF40 Sunscreen UVA-UVB Sunscreen with SolSci-XAVOBENZONE, OCTISALATE, AND OCTOCRYLENEMDSolarSciences812caa99-1e1e-4ab8-9f9a-fb3384c684dd2025-06-05WarningsExact identifier
ndc (package): 49358-556-01
ndc (product): 49358-556
ndc11 (package): 49358055601
spl id: 36d896f7-370c-c98b-e063-6294a90a70f6
spl set id: 812caa99-1e1e-4ab8-9f9a-fb3384c684dd

Reported adverse events (FAERS/openFDA)#

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