BELIF DEW GUARD - DAILY MINERAL SUNSCREEN BROAD SPECTRUM SPF 50- zinc oxide cream

belif Dew guard - daily mineral sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

belif Dew guard - daily mineral sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by LG H&H CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Zinc Oxide 17.46%

Purpose

Sunscreen

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.

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.

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

Directions

• Apply generously and evenly 15 minutes before sun exposure.
• Reapply at least every 2 hours.
• Use a water resistant sunscreen if swimming or sweating.
• 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 10 a.m. – 2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses.
• Children under 6 months: Ask a doctor.

Inactive Ingredients

Water, Dimethicone, Caprylyl Methicone, Butyloctyl Salicylate, Lauryl Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Dipropylene Glycol, Benzotriazolyl Dodecyl P-Cresol, Glycerin, Niacinamide, Polyglyceryl-6 Polyricinoleate, Disteardimonium Hectorite, 1,2-Hexanediol, Isostearic Acid, Magnesium Sulfate, Methyl Methacrylate Crosspolymer, Panthenol, Trimethylsiloxysilicate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Diphenylsiloxy Phenyl Trimethicone, Triethoxycaprylylsilane, Caprylic/Capric Triglyceride, Dimethicone/Polyglycerin-3 Crosspolymer, Fragrance++, Distearyldimonium Chloride, Dimethicone/Phenyl Vinyl Dimethicone Crosspolymer, Myristica Fragrans (Nutmeg) Extract, Melissa O­cinalis Flower/Leaf/Stem Water*, Rosmarinus O­cinalis (Rosemary) Leaf Water*, Sodium Hyaluronate+, Sodium Citrate, Butylene Glycol, Tocopherol, Cholesterol, Eucalyptus Globulus Leaf Extract*, Hydrolyzed Hyaluronic Acid+, Hydrogenated Lecithin, Alcohol Denat., Mentha Rotundifolia Leaf Extract*, Rosa Canina Fruit Extract*, Hyaluronic Acid+, Hydrolyzed Sodium Hyaluronate+, Hydroxypropyltrimonium Hyaluronate+, Sodium Acetylated Hyaluronate+, Cetearyl Alcohol, Stearic Acid, Thymus Vulgaris (Thyme) Leaf Extract*, Pentylene Glycol, Ceramide NP, Caprylyl Glycol, Ecklonia Cava Extract**, Hizikia Fusiforme Extract**, Laminaria Japonica Extract**, Ethylhexylglycerin, Ceramide NS, Phytosphingosine, Sodium Hyaluronate Crosspolymer+, Acetyl Hexapeptide-8, Ceramide AP, Ceramide AS, Desamido Collagen, Ceramide EOP, Limonene, Citronellol, Geraniol, Linalool, Citral.

(* belif original formula / + multi7-Hyaluron / ** Jeju-Haeyun Complex / ++ : Fragrance of botanical origin)

Other Information

Protect the product in this container from excessive heat and direct sun

Questions or comments?

Contact our Sun Specialists at 1-866-993-4709 or www.belifusa.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BELIF DEW GUARD - DAILY MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53208-740
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	17.46 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CERAMIDE NS (UNII: V7M2259XJM)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
NIACINAMIDE (UNII: 25X51I8RD4)
HYALURONIC ACID (UNII: S270N0TRQY)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
THYMUS VULGARIS (THYME) LEAF (UNII: GRX3499643)
DIMETHICONE/PHENYL VINYL DIMETHICONE CROSSPOLYMER (UNII: ST6ZC4KVH2)
CITRAL (UNII: T7EU0O9VPP)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ISOSTEARIC ACID (UNII: X33R8U0062)
NUTMEG (UNII: AEE24M3MQ9)
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393)
CHOLESTEROL (UNII: 97C5T2UQ7J)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
ECKLONIA CAVA (UNII: UXX2N5V39P)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DEHYDRATED ALCOHOL (UNII: 3K9958V90M)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
MAGNESIUM SULFATE (UNII: DE08037SAB)
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER (UNII: 2P2G24V6T9)
TOCOPHEROL (UNII: R0ZB2556P8)
ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
CERAMIDE NP (UNII: 4370DF050B)
CERAMIDE AP (UNII: F1X8L2B00J)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
PANTHENOL (UNII: WV9CM0O67Z)
LAMINARIA JAPONICA (UNII: WE98HW412B)
CITRONELLOL (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
LINALOOL (UNII: D81QY6I88E)
WATER (UNII: 059QF0KO0R)
DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
MELISSA OFFICINALIS FLOWERING TOP (UNII: 5JQG17B06J)
MENTHA X ROTUNDIFOLIA LEAF (UNII: K59TXG2L3U)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: H49Q67JS3B)
STEARIC ACID (UNII: 4ELV7Z65AP)
SARGASSUM FUSIFORME (UNII: X436TJ4A11)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53208-740-02	1 in 1 CARTON	04/11/2025
1	NDC: 53208-740-01	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	04/11/2025

Labeler - LG H&H CO., LTD. (688276187)