Rocky Mountain Sunscreen SPF 50 Spray

Manufacturer
Rocky Mountain | Inspec Solutions LLC
Effective date
2026-03-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:50:50

Label at a glance#

ProductSunscreen SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE
Label structure7 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. 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 risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures lncludlng: ■ limit time In the...

Label contents#

Full prescribing information#

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 white smoking or near heat or flame.

Do not useon damaged or broken skin.
When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Iswallowed, get medical help or contact a Polson Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

 ■ apply liberally 15 minutes before sun exposure.
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 risk, regularly use a
sunscreen with broad spectrum SPF of 15 or higher and other sun
protection measures lncludlng: ■ limit time In the sun, especlally
from 10am to 2pm ■ wear long-sleeved shirts, pants, hats, and
sunglasses ■ children under 6 months: ask a doctor ■ do not spray
directly Into face. Spray on hands then apply to face ■ use In
well-ventilated area.

Other information

OTHER SAFETY INFORMATION

protect this product from excessive
heat and direct sun ■ may stain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Butyloctyi Sallcylate, Ethyl Alcohol
Denatured, Polyester-8, Oryza Sativa (Rice Bran) Oil, VA/Butyl
Maleate/lsobomyl Acrylate Copolymer.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49757-010-06Sunscreen SPF 50170 g in 1 CONTAINERSPRAY1704
49757-010-09Sunscreen SPF 50453 g in 1 BOTTLESPRAY4534
49757-010-12Sunscreen SPF 50907 g in 1 CONTAINERSPRAY9074
49757-010-22Sunscreen SPF 503629 g in 1 CONTAINERSPRAY36294

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49757-01049757-010-06, 49757-010-12, 49757-010-22, 49757-010-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
Sunscreen SPF 50AVOBENZONE 3% , HOMOSALATE 10%,OCTISALATE 5%Rocky Mountain9647b817-653f-45e5-b71a-ee9ad82e84eb2026-03-18WarningsExact identifier
ndc (package): 49757-010-12
ndc (package): 49757-010-09
ndc (package): 49757-010-06
ndc (package): 49757-010-22
ndc (product): 49757-010
ndc11 (package): 49757001022
ndc11 (package): 49757001009
ndc11 (package): 49757001012
ndc11 (package): 49757001006
spl id: 4d4f240d-5656-cc29-e063-6294a90a7903
spl set id: 9647b817-653f-45e5-b71a-ee9ad82e84eb

Reported adverse events (FAERS/openFDA)#

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