FDA.reportPublic FDA data

Surface Sun SPF 50 Mineral Spray 2026 (IS0482-SS)

Manufacturer
Surface Products Corp | Inspec Solutions LLC
Effective date
2026-05-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:56:04

Label at a glance#

ProductSurface Sun SPF 50 Mineral Sunscreen
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

• Helps prevent sunburn.Higher SPF gives more sun protection.

Dosage and administration

Shake well before using • spray liberally and spread evenly by hand 15 minutes before sun exposure • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours • hold container 4 to 6 inches from the skin to apply • do not spray directly into face. Spray on hands then apply to face • do not apply in windy conditions • use in a well-ventilated area. • Sun Protectio...

Label contents#

Full prescribing information#

Active ingredients                 

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide  24%

Uses

INDICATIONS & USAGE SECTION

• Helps prevent sunburn.Higher SPF gives more sun protection.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Shake well before using • spray liberally and spread

evenly by hand 15 minutes before sun exposure • reapply: • after 80
minutes of swimming or sweating • immediately after towel drying
• at least every 2 hours • hold container 4 to 6 inches from the skin to
apply • do not spray directly into face. Spray on hands then apply to face
• do not apply in windy conditions • use in a well-ventilated area.
• 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 long-sleeve shirts, pants, hats, and
sunglasses. • children under 6 months: Ask a doctor.

Warnings

WARNINGS SECTION

For external use only.

Do not useon damaged or broken skin.
When using this product• keep out of eyes. Rinse with water to
remove. • Do not puncture or incinerate. Contents under pressure. Do
not store at temperatures above 120ºF.
Stop use and ask doctor if rash occurs.
Keep out of reach of children.If swallowed, get medical help or
contact a Poison Control Center immediately

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Inactive Ingredeints

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice
Butyloctyl Salicylate
C12-15 Alkyl Benzoate
C13-15 Alkane
Caprylic/Capric Triglyceride
Caprylyl Glycol
Diisostearoyl Polyglyceryl-3 Dimer Dilinoleate
Dimethicone
Ethylhexylglycerin
Glycerin
Hydrogen Dimethicone
Inulin
Isopropyl Myristate
Magnesium Chloride
Pentylene Glycol
Polyglyceryl-3 Oleate
Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate
Polyhydroxystearic Acid
Propanediol
Silica
Sodium Chloride
Sodium Phytate
Sorbitan Olivate
Synthetic Beeswax
Water

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
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72344-118-05Surface Sun SPF 50 Mineral Sunscreen142 g in 1 CANSPRAY1422

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72344-11872344-118-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOEV5VD430YW9IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CAPRYLYL GLYCOL00YIU5438UIACT
DIISOSTEAROYL POLYGLYCERYL-3 DIMER DILINOLEATEG3232Z5S2OIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN DIMETHICONE (30 CST)JF2ZJ6R2WDIACT
INULINJOS53KRJ01IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
PENTYLENE GLYCOL50C1307PZGIACT
POLYGLYCERYL-3 OLEATEXRQ165498BIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
PROPANEDIOL5965N8W85TIACT
SILICAETJ7Z6XBU4IACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM PHYTATE88496G1ERLIACT
SORBITAN OLIVATEMDL271E3GRIACT
SYNTHETIC BEESWAX08MNR5YE2RIACT
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
Surface Sun SPF 50 Mineral SunscreenZINC OXIDE 24%Surface Products Corp6f95de43-cb71-4ddd-b438-a35ee2e14fae2026-05-05WarningsExact identifier
ndc (package): 72344-118-05
ndc (product): 72344-118
ndc11 (package): 72344011805
spl id: 511866b5-dabc-1a2c-e063-6294a90a89fe
spl set id: 6f95de43-cb71-4ddd-b438-a35ee2e14fae

Reported adverse events (FAERS/openFDA)#

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