HYDROGLOW DAILY SUNSCREEN BROAD SPECTRUM SPF 50 UVA AND UVB- sunscreen spf 50 lotion

HydroGlow Daily Sunscreen BROAD SPECTRUM SPF 50 UVA and UVB by

Drug Labeling and Warnings

HydroGlow Daily Sunscreen BROAD SPECTRUM SPF 50 UVA and UVB by is a Otc medication manufactured, distributed, or labeled by IHerb, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HEALTH CLAIM

Idealove™ HydroGlow Daily Sunscreen SPF 50 provides lasting moisture to skin while shielding it from the sun. This weightless, gel-based formula melts seamlessly into skin, delivering an instant boost of hydration—no white cast, no greasy residue, just a fresh, dewy glow. A luxurious blend of Hyaluronic Acid helps to replenish and retain moisture, keeping skin smooth to the touch.

Infused with a complex of amino acids, skin vitality is boosted for a healthy-looking complexion. Powered by a trio of broad-spectrum UV filters, this sunscreen defends against harmful UVA and UVB rays while working overtime to nourish, plump, and fortify your skin barrier.

Broad Spectrum Facial Sunscreen

Protects against UVA & UVB

Unique Hydrating Gel Texture

Ceramides for Barrier Protection

Bisabolol for Sensitive Skin

Amino Acids for Boosted Skin Vitality

Fragrance-Free

100% Vegan

Cruelty-Free

DESCRIPTION

Made in the USA with global ingredients. Manufactured for: iHerb, LLC 17400 Laguna Canyon Rd., Suite 400 Irvine, CA 92618 info@idealovebeauty.com www.idealovebeauty.com LREV0525hgds ide10019

ACTIVE INGREDIENT

Active Ingredients Purpose

Avobenzone 3.0%....................Sunscreen

Homosalate 7.3%.....................Sunscreen

Octisalate 5.0%........................Sunscreen

PURPOSE

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 sun.

DO NOT USE

Do not use on damaged or broken skin

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

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

STOP USE

Stop use and ask a doctor if rash occurs.

STORAGE AND HANDLING

Other information

Store at 20°-25° (68°-77°F)

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

INACTIVE INGREDIENT

Inactive ingredients

Water, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Ethylhexyl Methoxycrylene, Dipropylene Glycol, Betaine, Shorea Stenoptera Seed Butter, VP/Hexadecene Copolymer, Ceramide NP, Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Hydrolyzed Sodium Hyaluronate, PCA, Sodium PCA, Sodium Acetylated Hyaluronate, Bisabolol, Centella Asiatica Leaf Extract, Arginine, Serine, Alanine, Glycine, Threonine, Proline, Valine, Histidine, Isoleucine, Phenylalanine, Aspartic Acid, Spirodela Polyrhiza Extract, Hydroxyacetophenone, Dibutyl Lauroyl Glutamide, Dibutyl Ethylhexanoyl Glutamide, Glycolipids, Dipotassium Glycyrrhizate, Sodium Lactate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Carbomer, Pentylene Glycol, Tromethamine, Ethylhexylglycerin, Sodium Benzoate, Phenoxyethanol.

DOSAGE & ADMINISTRATION

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-sleeved shirts, pants, hats, and sunglasses

Children under 6 months of age: Ask a doctor.

WARNINGS

Warnings For external use only

INDICATIONS & USAGE

Directions

Apply generously 15 minutes before sun exposure

Reapply at least every 2 hours

Use a water resistant sunscreen if swimming or sweating

PRINCIPAL DISPLAY PANEL

Idealove

HydroGlow Daily Sunscreen SPF 50 BROAD SPECTRUM SPF 50 UVA & UVB

100 mL / 3.3 fl oz

INGREDIENTS AND APPEARANCE

HYDROGLOW DAILY SUNSCREEN BROAD SPECTRUM SPF 50 UVA AND UVB 
sunscreen spf 50 lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82287-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7.3 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PSEUDOMONAS GLUCOSE FERMENTATION RHAMNOLIPIDS (UNII: PB22NX2CJL)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
BETAINE (UNII: 3SCV180C9W)
SHOREA STENOPTERA SEED BUTTER (UNII: 129R0X862G)
VP/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
BISABOLOL (UNII: 24WE03BX2T)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM PCA (UNII: 469OTG57A2)
SPIRODELA POLYRHIZA (UNII: BJS9J628MG)
ISOLEUCINE (UNII: 04Y7590D77)
THREONINE (UNII: 2ZD004190S)
PHENYLALANINE (UNII: 47E5O17Y3R)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
CERAMIDE NP (UNII: 4370DF050B)
ARGININE (UNII: 94ZLA3W45F)
VALINE (UNII: HG18B9YRS7)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
SODIUM LACTATE (UNII: TU7HW0W0QT)
PROLINE (UNII: 9DLQ4CIU6V)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
ASPARTIC ACID (UNII: 30KYC7MIAI)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
ALANINE (UNII: OF5P57N2ZX)
CARBOMER (UNII: 0A5MM307FC)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SERINE (UNII: 452VLY9402)
GLYCINE (UNII: TE7660XO1C)
TROMETHAMINE (UNII: 023C2WHX2V)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PCA (UNII: SZB83O1W42)
HISTIDINE (UNII: 4QD397987E)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82287-0002-2	1 in 1 CARTON	10/01/2025
1	NDC: 82287-0002-1	100 mL 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	10/01/2025

Labeler - IHerb, LLC (071369826)