HUSTLE BUTTER SPF 50 MINERAL SUNSCREEN

Manufacturer
H.B.D. DIST. INC.
Effective date
2026-10-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-10 01:03:38

Label at a glance#

ProductHUSTLE BUTTER SPF 50 MINERAL SUNSCREEN
Active ingredientZINC OXIDE
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 aging caused by the sun.

Dosage and administration

• Apply liberally and evenly 15 minutes prior to sun exposure. • Reapply after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours. • Children under 6 months of age: Ask a doctor. 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...

Storage and handling

• Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 24%

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 aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Do not use• on damaged or broken skin.  • on fresh tattoos.

When using this productkeep out of eyes. Rinse with water to remove.

Stop use and ask a doctorif rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help, or contact Poison Control right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally and evenly 15 minutes prior to sun exposure. • Reapply after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours. • Children under 6 months of age: Ask a doctor. 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-sleeved shirts, pants, hats, and sunglasses. 

Other information

STORAGE AND HANDLING SECTION

• Protect this product from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Caprylic/Capric Triglyceride, Polyhydroxystearic Acid, Water, Ethylhexyl Olivate, Squalane, Isoamyl Laurate, Lauryl Laurate, Sorbitan Olivate, Copernicia Cerifera (Carnauba) Wax, Oryza Sativa (Rice) Bran Wax, C13-15 Alkane, Disteardimonium Hectorite, Polyglyceryl-3 Polyricinoleate, Hydrogenated Rapeseed Oil, Capryloyl Glycerin/Sebacic Acid Copolymer, Silica, Propanediol, Citrullus Lanatus (Watermelon) Seed Oil, Butyrospermum Parkii (Shea) Butter, Rosa Canina Fruit Oil, Cocos Nucifera (Coconut) Oil, Helianthus Annuus (Sunflower) Seed Oil, Camellia Sinensis Leaf Extract, Oryza Sativa (Rice) Bran Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Helianthus Annuus (Sunflower) Extract, Tocopherol, Sodium Phytate, Phenoxyethanol, Ethylhexylglycerin, Sodium Chloride, Fragrance

Questions or comments?

OTC - QUESTIONS SECTION

+1-212-505-3222

You may also report serious side effects to this phone number.

Mon-Fri 9AM-5PM ET

SPL UNCLASSIFIED SECTION

PROFESSIONAL TATTOO CARE

BROAD SPECTRUM UVA UVB

WATER RESISTANT 80 MINS

SHEER FINISH

Distributed by H.B.D. Dist. Inc.
132 Crosby Street, New York, NY 10012

Contact Us: info@hustlebutter.com
www. hustlebutter.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunscreenLotion-1SunscreenLotion-1

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72014-20172014-201-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-03-10full-release2026-06-01 00:59:10

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
7afffb17-c0df-479a-a816-17c9977b236593e328b4-23dc-4484-aecb-5c41672bbf722025-03-10WarningsExact identifier
spl set id: 93e328b4-23dc-4484-aecb-5c41672bbf72

Reported adverse events (FAERS/openFDA)#

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