FDA.reportPublic FDA data

meg

Manufacturer
Meg Cosmetics Inc | HK Kolmar USA, LLC
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:28:22

Label at a glance#

Productmeg
Active ingredientOCTISALATE, OCTOCRYLENE, HOMOSALATE, AVOBENZONE
Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

  • Apply generously and evenly 15 minutes before sun exposure.
  • Children under 6 months of age: Ask a doctor.
  • Reapply at least every 2 hours.
  • Use a water-resistant sunscreen if swimming or sweating.

INACTIVE INGREDIENT SECTION

Water (Aqua)
Glycerin
Butyloctyl Salicylate
Propanediol
Dibutyl Adipate
Polymethylsilsesquioxane
Cetearyl Olivate
Caprylyl Methicone
1,2-Hexanediol
Pentylene Glycol
VP/Eicosene Copolymer
Sorbitan Olivate
Potassium Cetyl Phosphate
Panthenol
Glyceryl Stearate
Butylene Glycol
Cetearyl Alcohol
Polyacrylate Crosspolymer-6
Methylpropanediol
Ammonium Acryloyldimethyltaurate/VP Copolymer
Xanthan Gum
Ethylhexylglycerin
Undaria Pinnatifida Extract
Tromethamine
Spirulina Platensis Extract
Plankton Extract
Ecklonia Cava Extract
Codium Fragile Extract
Hyaluronic Acid
Polyether-1
Portulaca Oleracea Extract
Beta-Glucan
T-Butyl Alcohol
Tocopherol
Biosaccharide Gum-1

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • When used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

OTC - ACTIVE INGREDIENT SECTION

Homosalate 14.00%
Octocrylene 10.00%
Octisalate 4.50%
Avobenzone 2.80%

OTC - DO NOT USE SECTION

No “Do not use” statements apply for this product when used as directed.

WARNINGS SECTION

  • For external use only.
  • Do not use on damaged or broken skin.
  • When using this product, keep out of eyes. Rinse with water to remove.
  • Stop use and ask a doctor if rash occurs.
  • Keep out of reach of children.

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of immediate container labeling (inner tube), 50 mL, NDC 87225-001-01

50 mL Sun Shield Tube- NDC 87225-001-0150 mL Sun Shield Tube- NDC 87225-001-01

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87225-001-01meg50 g in 1 TUBECREAM502
87225-001-02meg1 in 1 CARTONCREAM12

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87225-00187225-001-01, 87225-001-02

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
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TROMETHAMINE023C2WHX2VIACT
ECKLONIA CAVAUXX2N5V39PIACT
HYALURONIC ACIDS270N0TRQYIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
XANTHAN GUMTTV12P4NEEIACT
VINYLPYRROLIDONE/EICOSENE COPOLYMER035MV9S1C3IACT
POLYETHER-1 (2800 MPA.S)6QR7NJP3G8IACT
PORTULACA OLERACEA WHOLED5J3623SV2IACT
T-BUTYL ALCOHOLMD83SFE959IACT
PANTHENOLWV9CM0O67ZIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
CODIUM FRAGILEMSE6FUU012IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CETEARYL ALCOHOL2DMT128M1SIACT
POLYACRYLATE CROSSPOLYMER-6Q7UI015FF9IACT
PROPANEDIOL5965N8W85TIACT
DIBUTYL ADIPATEF4K100DXP3IACT
GLYCERYL STEARATE230OU9XXE4IACT
UNDARIA PINNATIFIDAICV1OK7M1SIACT
TOCOPHEROLR0ZB2556P8IACT
BIOSACCHARIDE GUM-1BB4PU4V09HIACT
SPIRULINA PLATENSIS9L3TIH1UUEIACT
PENTYLENE GLYCOL50C1307PZGIACT
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
SORBITAN OLIVATEMDL271E3GRIACT
CETEARYL OLIVATE58B69Q84JOIACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
GLYCERINPDC6A3C0OXIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT

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
megALL DAY SOOTHE SUN SHIELD BROAD SPECTRUM SPF48Meg Cosmetics Inc4526bacf-6451-b297-e063-6294a90af71a2025-12-16WarningsExact identifier
ndc (package): 87225-001-01
ndc (package): 87225-001-02
ndc (product): 87225-001
ndc11 (package): 87225000102
ndc11 (package): 87225000101
spl id: 461ab06e-ef89-f3ce-e063-6394a90a567a
spl set id: 4526bacf-6451-b297-e063-6294a90af71a

Reported adverse events (FAERS/openFDA)#

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