FDA.reportPublic FDA data

Mine Line Coconut Sunscreen SPF 50

Manufacturer
Spa de Soleil
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:29:10

Label at a glance#

ProductMine Line Coconut Sunscreen SPF 50
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 24%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

WarningsWhen using this product

  • keep out of the eye area
  • rinse with water to remove
  • stop use and ask a doctor if rash or irritation develops
  • for external use onlyl
  • keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply thin layer over clean, dry skin. Massage well. Allow 15 minutes of complete penetration before sun exposure. Reapply every 1-2 hours & after swimming or sweating. Protect the product in this container from excessive heat.

INDICATIONS & USAGE SECTION

Uses
Provides high protection against sunburn.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Glycerin, C13-15 Alkane, Polyglyceryl-6 Polyricinoleate, Propanediol, Isododecane, Coconut Alkanes, Dicaprylyl Carbonate, Triheptanoin, Coco-Caprylate/Caprate, Caprylhydroxamic Acid, Polyglyceryl-10 Dioleate, Ectoin, Squalane, Sodium Chloride, Hydrogenated Phosphatidylcholine, Saccharomyces Ferment, Tocopheryl Acetate, Disteardimonium Hectorite, Dilinoleic Acid/Butanediol Copolymer, Lauroyl Lysine, Glyceryl Caprylate, Castor Oil/IPDI Copolymer, Propylene Carbonate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunscreenBoxSunscreenBox

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
124351b2-6dbf-42d0-9ea7-f0e299215f9aProduct name120210115

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-7301-1Mine Line Coconut Sunscreen SPF 50128 mL in 1 BOTTLE, PLASTICLOTION1282

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68062-730168062-7301-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
DILINOLEIC ACID/BUTANEDIOL COPOLYMER1F2S8T535OIACT
LAUROYL LYSINE113171Q70BIACT
WATER059QF0KO0RIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
C13-15 ALKANE114P5I43UJIACT
POLYGLYCERYL-6 POLYRICINOLEATEYPM0ZOC2HRIACT
PROPANEDIOL5965N8W85TIACT
ISODODECANEA8289P68Y2IACT
COCONUT ALKANES1E5KJY107TIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
TRIHEPTANOIN2P6O7CFW5KIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
POLYGLYCERYL-10 DIOLEATE598RES7AXXIACT
ECTOIN7GXZ3858RYIACT
SQUALANEGW89575KF9IACT
SODIUM CHLORIDE451W47IQ8XIACT
HYDROGENATED SOYBEAN PHOSPHATIDYLCHOLINEQHQ97HF0PYIACT
ZINC OXIDESOI2LOH54ZACTIB
CASTOR OIL/IPDI COPOLYMERGSA2TXZ34GIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
PROPYLENE CARBONATE8D08K3S51EIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT

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
Mine Line Coconut Sunscreen SPF 50ZINC OXIDESpa de Soleil4642b1cc-43b1-6997-e063-6394a90ac7642025-12-29WarningsExact identifier
ndc (package): 68062-7301-1
ndc (product): 68062-7301
ndc11 (package): 68062730101
spl id: 471fc473-6bd4-8f97-e063-6294a90a523b
spl set id: 4642b1cc-43b1-6997-e063-6394a90ac764

Reported adverse events (FAERS/openFDA)#

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