FDA.reportPublic FDA data

Expedition BackCountry SPF 30 Spray

Manufacturer
Tropical Seas, Inc.
Effective date
2025-11-04
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:42:04

Label at a glance#

ProductExpedition BackCountry SPF 30
Active ingredientOCTOCRYLENE, OCTISALATE, AVOBENZONE
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 do not spray directly on face - spray into hands and apply to face hold approximately 4 - 6 inches from skin to spray rub into skin evenly to ensure appropriate coverage use in a well-ventilated area avoid inhaling or exposing others to spray do not apply in windy conditions reapply: after 80 minutes of swimming or sweating immediately after towel drying at least ever...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 5.0%

Octisalate 3.0%

Avobenzone 2.5%

Purpose

OTC - PURPOSE SECTION

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

Flammable: Do not use near heat, flame, or while smoking

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.
  • Do not puncture or incinerate. Contents under pressure.
  • Do not store at temperatures above 120° F

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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • do not spray directly on face - spray into hands and apply to face
  • hold approximately 4 - 6 inches from skin to spray
  • rub into skin evenly to ensure appropriate coverage
  • use in a well-ventilated area
  • avoid inhaling or exposing others to spray
  • do not apply in windy conditions
  • reapply:
    • after 80 minutes of 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 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
  • children under 6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

sd alcohol 40-b, deionized water, lauryl lactate, cyclopentasiloxane, c12-15 alcohols benzoate, acrylates octylacrylamide copolymer, octyldodecyl neopentanoate, octyl dodecyl citrate crosspolymer, phenethyl benzoate, citronella oil, eucalyptus oil, fir needle oil, lavandin oil, litsea oil, camphor oil, patchouli oil, yara yara, and orange oil.

Other Information

SPL UNCLASSIFIED SECTION

  • protect this product from excessive cold, heat, and direct sun.
  • store at temp below 90º F and avoid long term storage
  • may stain fabrics or surfaces

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-368-7327

Principal Display Panel - Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

180ml NDC 52854-326-01

NDC 52854-326-01NDC 52854-326-01

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130079608913265GTIN-13: 0079608913265
EAN-13: 0079608913265
GTIN-12: 079608913265
UPC-A: 079608913265
GTIN storage (14 digits): 00079608913265		EBC30spray6oz.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52854-326-01Expedition BackCountry SPF 30180 mL in 1 CANSPRAY1806

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52854-32652854-326-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ABIES BALSAMEA LEAF OIL2FGT9T2SQCIACT
EUCALYPTUS OIL2R04ONI662IACT
ACHILLEA MILLEFOLIUM ROOT OIL0S45F449MJIACT
LITSEA OIL2XIW34BN6OIACT
PHENETHYL BENZOATE0C143929GKIACT
CYCLOMETHICONE 50THT5PCI0RIACT
LAURYL LACTATEG5SU0BFK7OIACT
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW)JU3XHR8VWKIACT
OCTYLDODECYL CITRATE CROSSPOLYMERX323T6QO4MIACT
ALCOHOL3K9958V90MIACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
CITRONELLA OILQYO8Q067D0IACT
POGOSTEMON CABLIN LEAF OILF3IN55X5POIACT
LAVANDIN OIL9RES347CKGIACT
CAMPHOR OIL75IZZ8Y727IACT
ORANGE OILAKN3KSD11BIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-11-01full-release2026-06-01 00:33:29

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
Expedition BackCountry SPF 30OCTOCRYLENE, OCTISALATE, AND AVOBENZONETropical Seas, Inc.b5e4e63c-3e51-0a78-e053-2a95a90abd872025-11-04WarningsExact identifier
ndc (package): 52854-326-01
ndc (product): 52854-326
ndc11 (package): 52854032601
spl id: 42c9eb56-f5ec-4d86-e063-6394a90a0c01
spl set id: b5e4e63c-3e51-0a78-e053-2a95a90abd87

Reported adverse events (FAERS/openFDA)#

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