FDA.reportPublic FDA data

Dead Down Wind Sunscreen

Manufacturer
DEAD DOWN WIND, LLC | Ec Labs Inc
Effective date
2022-01-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:11:36

Label at a glance#

ProductDead Down Wind Sunscreen
Active ingredientOCTINOXATE, AVOBENZONE, HOMOSALATE, OCTISALATE
Label structure9 sections

Indications and uses

helps prevent sunburn

Dosage and administration

Apply liberally to all exposed skin 15 minutes before sun exposure. Reapply every 2 hours. Use a water resistant sunscreen if swimming or sweating. 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, esp...

Storage and handling

Protect the product in this container from excessive heat and direct sun.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone............1.6%

Homosalate.............2.1%

Octinoxate...............2.1%

Octisalate................2.1%

Purpose

OTC - PURPOSE SECTION

Avobenzone............1.6% - Sunscreen

Homosalate.............2.1% - Sunscreen

Octinoxate...............2.1% - Sunscreen

Octisalate................2.1% - Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps 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 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 liberally to all exposed skin 15 minutes before sun exposure.
  • Reapply every 2 hours.
  • Use a water resistant sunscreen if swimming or sweating.
  • 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-sleeved shirts, pants, hats, and sunglasses.
  • For children under 6 months of age: ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carthamus Tinctorius (Safflower) Oleosomes, Dipropylene Glycol Dibenzoate, Glycerin, Ammonium Acryloyldimethyltaurate/VP Copolymer, Citronellyl Methylcrotonate, Phenoxyethanol, Ethylhexylglycerin, Sodium Hydroxide, Xanthan Gum

Other information

STORAGE AND HANDLING SECTION

  • Protect the product in this container from excessive heat and direct sun.

Questions?

OTC - QUESTIONS SECTION

Call toll free 1-888-486-8339

MONDAY-FRIDAY, 8:30am-5:00pm EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BROAD SPECTRUM

SPF 30

DEAD DOWN WIND

UNSCENTED

SUN

SCREEN

UNSCENTED

SUN PROTECTION

FOR HUNTERS

3 FL OZ (88.72 mL)

11

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
81502-00281502-002-01

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
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES9S60Q72309IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
SODIUM HYDROXIDE55X04QC32IIACT
OCTINOXATE4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
GLYCERINPDC6A3C0OXIACT
CITRONELLYL METHYLCROTONATEK61O222P3DIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DIPROPYLENE GLYCOL DIBENZOATE6OA5ZDY41OIACT
XANTHAN GUMTTV12P4NEEIACT

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
0d99b4b7-073a-782d-e063-6394a90a723dd6766cb4-313e-e4d6-e053-2a95a90a5fc82023-12-28WarningsExact identifier
spl set id: d6766cb4-313e-e4d6-e053-2a95a90a5fc8

Reported adverse events (FAERS/openFDA)#

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