MEG- all day soothe sun shield broad spectrum spf48 cream

meg by

Drug Labeling and Warnings

meg by is a Otc medication manufactured, distributed, or labeled by Meg Cosmetics Inc, HK Kolmar USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

• 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

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

• 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.

ACTIVE INGREDIENT

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

DO NOT USE

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

WARNINGS

• 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.

PURPOSE

Sunscreen

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

MEG 
all day soothe sun shield broad spectrum spf48 cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87225-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	140 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	28 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TROMETHAMINE (UNII: 023C2WHX2V)
ECKLONIA CAVA (UNII: UXX2N5V39P)
HYALURONIC ACID (UNII: S270N0TRQY)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
XANTHAN GUM (UNII: TTV12P4NEE)
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
POLYETHER-1 (2800 MPA.S) (UNII: 6QR7NJP3G8)
PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
T-BUTYL ALCOHOL (UNII: MD83SFE959)
PANTHENOL (UNII: WV9CM0O67Z)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
CODIUM FRAGILE (UNII: MSE6FUU012)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)
PROPANEDIOL (UNII: 5965N8W85T)
DIBUTYL ADIPATE (UNII: F4K100DXP3)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S)
TOCOPHEROL (UNII: R0ZB2556P8)
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
WATER (UNII: 059QF0KO0R)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
GLYCERIN (UNII: PDC6A3C0OX)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87225-001-02	1 in 1 CARTON	12/03/2025
1	NDC: 87225-001-01	50 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/03/2025

Labeler - Meg Cosmetics Inc (128996905)

Establishment
Name	Address	ID/FEI	Business Operations
HK Kolmar USA, LLC		809172885	manufacture(87225-001)