FDA.reportPublic FDA data

Dynamic Broad Spectrum Sunscreen SPF 55

Manufacturer
Prescriber's Choice, LLC
Effective date
2021-03-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:48:28

Label at a glance#

ProductDynamic Sunscreen Broad Spectrum SPF 55
Active ingredientOCTINOXATE, ZINC OXIDE
Label structure9 sections

Indications and uses

Help prevent sunburn.

Dosage and administration

Apply liberally and evenly 15 minutes before sun exposure. For children under 6 months of age: Ask a doctor. Reapply: At least 80 minutes after swimming or sweating, immediately after towel drying, at least every 2 hours. 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 high...

Storage and handling

Store at controlled temperature 15C – 30C (59F-86F). Protect the product in this container from excessive heat and direct sun.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.5%

Zinc Oxide 4.8%

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

USES

INDICATIONS & USAGE SECTION

Help prevent sunburn.

WARNINGS

WARNINGS SECTION

For external use only.

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 a doctor if rash or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply liberally and evenly 15 minutes before sun exposure. 1Reapply:

At least 80 minutes after swimming or sweating, immediately after towel drying, at least every 2 hours.

  • 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 a.m. – 2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses.

1 For children under 6 months of age: Ask a doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Hydrogenated Polybutene, Octyl Stearate, Polyglyceryl-4-Isostearate, Aloe Barbadensis Leaf Extract, Isopropyl Palmitate, Cyclomethicone, Sunflower Oil, Hydrogenated Microcrystalline Wax, Cetyl Dimethicone Copolyol, Cetyl Dimethicone, Hydrogenated Castor Oil, Sodium Chloride, Polyglyceryl-3-Oleate, Silica, Hexyl Laurate, Triethoxycaprylylsilane, Capryly Glycol, Methylisothiazolinone.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store at controlled temperature 15C – 30C (59F-86F). Protect the product in this container from excessive heat and direct sun.

Pescriber's Choice Dynamic Sunscreen Broad Spectrum SPF 55 Sun Protection 4fl oz (120ml)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pescriber's Choice
Dynamic Sunscreen Broad Spectrum SPF 55
Sun Protection
4fl oz (120ml) Pescriber's Choice Dynamic Sunscreen Broad Spectrum SPF 55 Sun Protection 4fl oz (120ml)Pescriber's Choice Dynamic Sunscreen Broad Spectrum SPF 55 Sun Protection 4fl oz (120ml)

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71876-561271876-5612-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOCETYL STEARATE3RJ7186O9WIACT
SORBITOL506T60A25RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CYCLOMETHICONE 50THT5PCI0RIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
ALCOHOL3K9958V90MIACT
OCTISALATE4X49Y0596WIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VINYLPYRROLIDONE/EICOSENE COPOLYMER035MV9S1C3IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)86FQE96TZ4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
BETULA PUBESCENS BARK3R504894L9IACT
GARDEN CRESS SPROUTPWQ18YNR62IACT
SAGE065C5D077JIACT
COLA ACUMINATA SEED1F8VIW1479IACT
CAMELLIA OLEIFERA LEAF5077EL0C60IACT
ALOE VERA LEAFZY81Z83H0XIACT
XANTHAN GUMTTV12P4NEEIACT
ISOMALTS870P55O2WIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SODIUM BENZOATEOJ245FE5EUIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
OCTINOXATE4Y5P7MUD51ACTIB
ZINC OXIDESOI2LOH54ZACTIB

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e7b3093c-be0b-8f42-e053-2a95a90a68d6b865825e-402a-a4d3-e053-2a95a90a35df2022-09-02WarningsExact identifier
spl set id: b865825e-402a-a4d3-e053-2a95a90a35df

Reported adverse events (FAERS/openFDA)#

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