Mineral Lip Firecracker

Manufacturer
Bell International Laboratories, Inc.
Effective date
2017-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:10:51

Label at a glance#

ProductMineral Lip Firecracker SPF 30 Broad Spectrum
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
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 & again after 40 minutes of swimming or sweating. Apply at least every 2 hours. Sun Protection Measures - to decrease your risk of cancer and early skin aging, 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 10am-2pm and wear long-sleeved shirts, pants, hats a...

Label contents#

Full prescribing information#

Acitve Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 2.8%, Zinc Oxide 1.4%

Purpose

OTC - PURPOSE SECTION

Sunscreens

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.

Do not use on damaged or broken skin

When using this product keep out of eyes.

Stop use and ask doctor if skin 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 & again after 40 minutes of swimming or sweating. Apply at least every 2 hours.

Sun Protection Measures - to decrease your risk of cancer and early skin aging, 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 10am-2pm and wear long-sleeved shirts, pants, hats and sunglasses

Children under 6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Beeswax (ORGANIC), Butyrospermum Parkii (ORGANIC Shea Butter), Carmine, Cocos Nucifera (ORGANIC Coconut) Oil, Copernicia Cerifera (ORGANIC Carnauba) Wax, Flavor, Iron Oxides, Jojoba Esters, Octyldodecyl Oleate, Olea Europaea (ORGANIC Olive) Fruit Oil, Oryzanol, Schinziophyton Rautanenii Kernel Oil (ORGANIC), Silica, Theobroma Grandiflorum Seed Butter (ORGANIC), Tocopherol

Other Safety Informaiton

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-18076150-180-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5cc391be-ac82-4dca-e053-2a91aa0aedcc5cc391be-ac81-4dca-e053-2a91aa0aedcc2017-10-30WarningsExact identifier
spl id: 5cc391be-ac82-4dca-e053-2a91aa0aedcc
spl set id: 5cc391be-ac81-4dca-e053-2a91aa0aedcc

Reported adverse events (FAERS/openFDA)#

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