FDA.reportPublic FDA data

SPF 50 Mineral Sunscreen Kids

Manufacturer
S&C Hampton Sun LLC | Inspec Solutions
Effective date
2026-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:34:10

Label at a glance#

ProductSPF 50 Mineral Sunscreen Kids
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

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 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 includ...

Label contents#

Full prescribing information#

Active Ingredients                       Purpose

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 14.69%                        Sunscreen

Uses

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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

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 children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Butyloctyl Salicylate
Butyrospermum Parkii (Shea) Oil
C12-15 Alkyl Benzoate
Caprylic/Capric Triglyceride
Dibutyl Ethylhexanoyl Glutamide
Dibutyl Lauroyl Glutamide
Ethylhexyl Methoxycrylene
Fragrance
Octyldodecanol
Rebaudioside A
Simmondsia Chinensis (Jojoba) Seed Oil
Sodium Hyaluronate
Tocopheryl Acetate
Triethoxycaprylylsilane
Vitis Vinifera (Grape) Seed Oil
VP/Hexadecene Copolymer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87170-005-01SPF 50 Mineral Sunscreen Kids13 g in 1 CONTAINERSTICK132

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87170-00587170-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
DIBUTYL ETHYLHEXANOYL GLUTAMIDE0IAF2L30VSIACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
FRAGRANCE LAVENDER ORC18009791B40MIN2W5IACT
OCTYLDODECANOL461N1O614YIACT
REBAUDIOSIDE AB3FUD0528FIACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
SODIUM HYALURONATEYSE9PPT4THIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
VITIS VINIFERA (GRAPE) SEED OIL930MLC8XGGIACT
VP/HEXADECENE COPOLYMERKFR5QEN0N9IACT
ZINC OXIDESOI2LOH54ZACTIM

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
SPF 50 Mineral Sunscreen KidsZINC OXIDE 14.69%S&C Hampton Sun LLC0bdb7d15-dc52-4e23-9417-fe73f17f61102026-01-20WarningsExact identifier
ndc (package): 87170-005-01
ndc (product): 87170-005
ndc11 (package): 87170000501
spl id: 48d91eed-7bff-4240-e063-6394a90a4a82
spl set id: 0bdb7d15-dc52-4e23-9417-fe73f17f6110

Reported adverse events (FAERS/openFDA)#

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