Black Girl Sunscreen SPF 50

Manufacturer
Black Girl Sunscreen | Inspec Solutions
Effective date
2025-09-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:15:00

Label at a glance#

ProductBlack Girl Sunscreen SPF 50
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure7 sections

Label contents#

Full prescribing information#

Active ingredients                   Purpose

OTC - ACTIVE INGREDIENT SECTION

Homosalate 10.00%
Octocrylene 10.00%                 Sunscreen
Octisalate 5.00%
Avobenzone 3.00%

INDICATIONS & USAGE SECTION

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 & ADMINISTRATION SECTION

Directions• apply liberally to cool, dry skin
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 this risk, regularly
use a sunscreen with a broad spectrum SPF of 15
or higher and other sun protection measures
including: • limit time in the sun,especially from
10 a.m. - 2. p.m. • wear a long-sleeve shirts,
pants, hats, and sunglasses. • children under 6
months: Ask a doctor.

WARNINGS SECTION

Warnings
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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

C12-15 Alkyl Benzoate
Caprylic/Capric Triglyceride
Cetyl Alcohol
Dimethicone
Ethylhexyl Methoxycrylene
Euphorbia Cerifera (Candililla) Wax
Humulus Lupulus (Hops) Extract
Lauric Acid
Myristic Acid
Neopentyl Glycol Diethylhexanoate
Ozokerite
Palmitic Acid
Polyethylene
Silica
Stearic Acid
Synthetic Beeswax

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84204-0015-1Black Girl Sunscreen SPF 5018 g in 1 CONTAINERSTICK182

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84204-001584204-0015-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
Black Girl Sunscreen SPF 50HOMOSALATE 10.00% OCTOCRYLENE 10.00% OCTISALATE 5.00% AVOBENZONE 3.00%Black Girl Sunscreenfed22570-e0ae-43e1-b6ce-1f0ad01684c32025-09-26WarningsExact identifier
ndc (package): 84204-0015-1
ndc (product): 84204-0015
ndc11 (package): 84204001501
spl id: 3fb49f59-5ce2-da76-e063-6294a90af1f7
spl set id: fed22570-e0ae-43e1-b6ce-1f0ad01684c3

Reported adverse events (FAERS/openFDA)#

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