CANNON BALM 140

Manufacturer
DUKE CANNON SUPPLY CO.
Effective date
2023-03-16
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:34:33

Label at a glance#

ProductCANNON BALM 140
Active ingredientOCTINOXATE, AVOBENZONE, OCTISALATE, OXYBENZONE
Label structure10 sections

Storage and handling

Other Information Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Octinoxate (7.5%)

Octisalate (5.0%)

Avobenzone  (4.0%)

Oxybenzone (4.0%)

OTC - PURPOSE SECTION

Purpose:

Sunscreen

Sunscreen

Sunscreen

Sunscreen

INDICATIONS & USAGE SECTION

Uses:

•Helps prevent sunburn and chapped lips

WARNINGS SECTION

Warnings:

For external use only.

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 value 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

Children under 6 months:  ask a doctor

When using this product:

•Keep out of eyes

•Rinse with water to remove

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.

DOSAGE & ADMINISTRATION SECTION

Directions:

•Apply liberally and reapply every 2 hours for sunburn protection

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Organic Baobab Oil, Organic Beeswax, Organic Blood Orange Essential Oil, Organic, Calendula Extract,

Castor Oil, Ceresine Wax, Hydrated Silica, Hydroxystearic/Linoleic/Linolenic/Oleic Polyglycerides,

Natural Flavor, Organic Olive Oil, Organic Peppermint Essential Oil, Polyisobutene, Rice Bran Wax,

Organic Rosemary Extract, Organic Stevia, Organic Tea Tree Essential Oil, Vitamin E.

STORAGE AND HANDLING SECTION

Other Information

Protect this product from excessive heat and direct sun.

OTC - QUESTIONS SECTION

Questions or Comments?

Call 1.855.354.4438

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71782-140-012023-03-16C16284748780-1ba0f9c33-2e1d-a910-e053-dadaa90a0b85fbc3d22b-c7d6-474f-ba3f-89d6a5853e6c
71782-140-012021-01-29C16284748780-1ba0f9c33-2e1d-a910-e053-dadaa90a0b85fbc3d22b-c7d6-474f-ba3f-89d6a5853e6c

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71782-14071782-140-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
f709c4fe-0b52-8f2c-e053-6394a90a6395fbc3d22b-c7d6-474f-ba3f-89d6a5853e6c2023-03-16WarningsExact identifier
spl id: f709c4fe-0b52-8f2c-e053-6394a90a6395
spl set id: fbc3d22b-c7d6-474f-ba3f-89d6a5853e6c

Reported adverse events (FAERS/openFDA)#

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