FDA.reportPublic FDA data

SPF 40 Quick Dry Body Spray

Manufacturer
MD Solar Sciences
Effective date
2012-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:32:26

Label at a glance#

ProductMDSolarSciences SPF 40 Quick Dry
Active ingredientAvobenzone, Octisalate, Octocrylene
Label structure9 sections

Indications and uses

Helps prevent sunburn Higher SPF gives more sunburn protection Retains SPF after 80 minutes of activity in water

Dosage and administration

Apply generously 30 minutes before sun exposure and as needed Do not spray on face Spray on hands and rub well into face and scalp Reapply every 2 hours, or after swimming, excessive perspiration, towel drying or extended sun exposure Children under 6 months of age: ask a doctor Effective sun protection for children under 2 years of age is strongly recommended

Storage and handling

Use in well ventilated areas Do not puncture or incinerate Contents under pressure Do not store above 120°F/48°C Avoid long term storage above 104°F/40°C FLAMMABLE Do not use near heat, flame or while smoking

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients:Purpose
Avobenzone 3.00%Sunscreen
Octisalate 5.00%Sunscreen
Octocrylene 2.75%Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • Higher SPF gives more sunburn protection
  • Retains SPF after 80 minutes of activity in water

Warnings

WARNINGS SECTION

OTC - DO NOT USE SECTION

For external use only.

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 a doctor if 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 Poison Control Center right away.

STORAGE AND HANDLING SECTION

  • Use in well ventilated areas
  • Do not puncture or incinerate
  • Contents under pressure
  • Do not store above 120°F/48°C
  • Avoid long term storage above 104°F/40°C
  • FLAMMABLE
  • Do not use near heat, flame or while smoking

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply generously 30 minutes before sun exposure and as needed
  • Do not spray on face
  • Spray on hands and rub well into face and scalp
  • Reapply every 2 hours, or after swimming, excessive perspiration, towel drying or extended sun exposure
  • Children under 6 months of age: ask a doctor
  • Effective sun protection for children under 2 years of age is strongly recommended

Other information

SPL UNCLASSIFIED SECTION

Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

  • 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, EDTA, Phytic Acid, Phyllanthus Emblica Fruit Extract, Tetrahexyldecyl Ascorbate, Trisodium Ethylenediamine Disuccinate

PRINCIPAL DISPLAY PANEL - 148 mL Can Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MDSolarSciences

SPF 40
with
SolSciX

Broad Spectrum
UVA-UVB Sunscreen

Quick Dry
Body Spray

EASY APPLICATION

for Active Lifestyles

Light & Non-Greasy
Very Water Resistant
No Fragrance

Dermatologist Developed

Includes our
SolALERT
UV Index
Card

148 mL- 5.0 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
49358-544-012019-11-13C16284748780-197449f38-d3f4-f6ea-e053-dbdaa90aa703SPF 40 Quick Dry Body Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49358-544-01MDSolarSciences SPF 40 Quick Dry148 mL in 1 CANSPRAY1481
49358-544-01MDSolarSciences SPF 40 Quick Dry1 in 1 CARTONSPRAY11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49358-544MDSOLARSCIENCES SPF 40 QUICK DRY (AVOBENZONE, OCTISALATE, AND OCTOCRYLENE) SPRAY [MD SOLAR SCIENCES]1Legacy NDC, 2 package rows20120630_6ec57abd-c60e-4994-8d82-a2627eea7336.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AvobenzoneACTIVE INGREDIENTG63QQF2NOX1
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
AvobenzoneACTIVE MOIETYG63QQF2NOX1
OctisalateACTIVE MOIETY4X49Y0596W1
OctocryleneACTIVE MOIETY5A68WGF6WM1
Butyloctyl SalicylateINACTIVE INGREDIENT2EH13UN8D31
Diisopropyl AdipateINACTIVE INGREDIENTP7E6YFV72X1
Edetic AcidINACTIVE INGREDIENT9G34HU7RV01
Fytic AcidINACTIVE INGREDIENT7IGF0S7R8I1
Phyllanthus Emblica FruitINACTIVE INGREDIENTYLX4CW25761
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 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49358-54449358-544-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
AvobenzoneG63QQF2NOXACTIB
Octisalate4X49Y0596WACTIB
Octocrylene5A68WGF6WMACTIB
Butyloctyl Salicylate2EH13UN8D3IACT
Diisopropyl AdipateP7E6YFV72XIACT
Edetic Acid9G34HU7RV0IACT
Fytic Acid7IGF0S7R8IIACT
Phyllanthus Emblica FruitYLX4CW2576IACT
Tetrahexyldecyl Ascorbate9LBV3F07AZIACT
Trisodium Ethylenediamine DisuccinateYA22H34H9QIACT

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 · 20 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XLOTION / TOPICAL250 mgExact identifier — unii candidate
7 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0GEL / TOPICAL0.1 %w/wExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0CREAM / TOPICAL0.5 %w/wExact identifier — unii candidate
13 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XSOLUTION / TOPICAL815 mgExact identifier — unii candidate
7 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0INJECTION, SOLUTION / INTRAMUSCULAR2 mgExact identifier — unii candidate
13 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XAEROSOL, FOAM / TOPICAL200 mgExact identifier — unii candidate
7 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XCREAM / TOPICAL170 mgExact identifier — unii candidate
7 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0INJECTION, SOLUTION / SUBCUTANEOUS2 mgExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0INJECTION, SOLUTION / INTRAVENOUS2 mgExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0TABLET / ORAL4 mgExact identifier — unii candidate
13 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XGEL / TOPICAL150 mgExact identifier — unii candidate
7 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SHAMPOO / TOPICAL0.2 %w/wExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SUSPENSION / AURICULAR (OTIC)NAExact identifier — unii candidate
13 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XGEL / TRANSDERMAL1.5 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0INJECTION, SOLUTION / SUBMUCOSAL0.03 %w/vExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SOLUTION / TOPICAL0.5 %w/wExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SUPPOSITORY / RECTAL7 mgExact identifier — unii candidate
13 equally ranked IID candidates
Diisopropyl AdipateDIISOPROPYL ADIPATEP7E6YFV72XSPRAY / TOPICAL360 mgExact identifier — unii candidate
7 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0TABLET, FILM COATED / ORAL0.2 mgExact identifier — unii candidate
13 equally ranked IID candidates
Edetic AcidEDETIC ACID9G34HU7RV0SUSPENSION / TOPICAL0.06 %w/vExact identifier — unii candidate
13 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
e8b49e5d-db0c-44d0-a435-4bde9abcf38a6ec57abd-c60e-4994-8d82-a2627eea73362012-04-24WarningsExact identifier
spl id: e8b49e5d-db0c-44d0-a435-4bde9abcf38a
spl set id: 6ec57abd-c60e-4994-8d82-a2627eea7336

Reported adverse events (FAERS/openFDA)#

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