FDA.reportPublic FDA data

Hampton Sun SPF 50 Mineral Lotion

Manufacturer
S&C Hampton Sun | Inspec Solutions
Effective date
2026-01-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:34:57

Label at a glance#

ProductZinc Oxide 20%
Active ingredientZINC OXIDE
Label structure6 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 evenly to face and neck 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 value of 15 or higher and other sun protection measures includin...

Label contents#

Full prescribing information#

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply evenly to face and neck 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 value of 15 or higher and other sun
protection measures including: Limit time in the sun, especially from
10a.m.– 2p.m. . Wear long-sleeve shirts, pants, hats, and sunglasses.
. Children under 6 months: Ask a doctor.

Warnings For external use only.

WARNINGS SECTION

Do not useon damaged or broken skin.
When using this product• keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor ifrash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice
Ascorbyl Tetraisopalmitate
Butylene Glycol
Butyloctyl Salicylate
Caprylic/Capric Triglyceride
Carbomer
Ceramide AP
Ceramide EOP
Ceramide NP
Cetearyl Olivate
Cholesterol
Citric Acid
Dicaprylyl Carbonate
Dimethicone
Ethylhexyl Methoxycrylene
Ethylhexylglycerin
Fragrance
Helianthus Annuus (Sunflower) Seed Oil
Hydrogenated Castor Oil
Isopropyl Myristate
Magnesium Sulfate
Niacinamide
Persea Gratissima
Phenoxyethanol
Phytosphingosine
Polyglyceryl-3 Polyricinoleate
Polyhydroxystearic Acid
Potassium Sorbate
Propylene Glycol
Sodium Benzoate
Sodium Hyaluronate
Sodium Lauroyl Lactylate
Sorbitan Oleate
Sorbitan Olivate
Synthetic Beeswax
Tocopheryl Acetate
VP/Hexadecene Copolymer
Water
Xanthan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image 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
87170-006-10Zinc Oxide 20%946 mL in 1 BOTTLELOTION9461

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87170-00687170-006-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
ASCORBYL TETRAISOPALMITATE47143LT58AIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CARBOMER0A5MM307FCIACT
CERAMIDE APF1X8L2B00JIACT
CERAMIDE 988KCS7120EIACT
CERAMIDE NP4370DF050BIACT
CETEARYL OLIVATE58B69Q84JOIACT
CHOLESTEROL97C5T2UQ7JIACT
CITRIC ACID2968PHW8QPIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
CASTOR OILD5340Y2I9GIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
NIACINAMIDE25X51I8RD4IACT
PERSEA GRATISSIMA (AVOCADO) OIL6VNO72PFC1IACT
PHENOXYETHANOLHIE492ZZ3TIACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM HYALURONATEYSE9PPT4THIACT
SODIUM LAUROYL LACTYLATE7243K85WFOIACT
SORBITAN OLEATE06XEA2VD56IACT
SORBITAN OLIVATEMDL271E3GRIACT
SYNTHETIC BEESWAX08MNR5YE2RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VP/HEXADECENE COPOLYMERKFR5QEN0N9IACT
WATER059QF0KO0RIACT
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
Zinc Oxide 20%SUNSCREEN SPF 50 MINERALS&C Hampton Sun4960930e-a1bf-d850-e063-6294a90a40842026-01-27WarningsExact identifier
ndc (package): 87170-006-10
ndc (product): 87170-006
ndc11 (package): 87170000610
spl id: 4960925b-fe36-43b0-e063-6394a90a42cc
spl set id: 4960930e-a1bf-d850-e063-6294a90a4084

Reported adverse events (FAERS/openFDA)#

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