EUCERIN RADIANT TONE- avobenzone, homosalate, octisalate, octocrylene lotion

Eucerin Radiant Tone by

Drug Labeling and Warnings

Eucerin Radiant Tone by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Avobenzone 3%

Homosalate 8%

Octisalate 4.5%

Octocrylene 9%

PURPOSE

Purpose

Sunscreens

INDICATIONS & USAGE

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

Warnings

For external use only

.

DO NOT USE

Do not use on damaged or broken skin.

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

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.

DOSAGE & ADMINISTRATION

Directions

For sunscreen use:

apply liberally 15 minutes before sun exposure

use a water resistant sunscreen if swimming or sweating

reapply at least every 2 hours

children under 6 months of age: Ask a doctor

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 of age: Ask a doctor.

OTHER SAFETY INFORMATION

Other information

protect this product from excessive heat and direct sun

INACTIVE INGREDIENT

Inactive ingredients

Water, Glycerin, Alcohol Denat., Glyceryl
Stearate, Silica, Butylene Glycol
Dicaprylate/Dicaprate, C12-15 Alkyl
Benzoate, Cetearyl Alcohol, Dibutyl Adipate,
Silica Dimethyl Silylate, Tocopherol,
Isobutylamido Thiazolyl Resorcinol,
Glycyrrhiza Inflata Root Extract, Sodium
Stearoyl Glutamate, Glyceryl Behenate,
Polyglyceryl-6 Octastearate, Xanthan Gum,
Phenoxyethanol, Ethylhexylglycerin,
Disodium EDTA, Sodium Chloride, Fragrance.

PRINCIPAL DISPLAY PANEL

Eucerin

Dark Spot Corrector

Radiant Tone

Daily Lotion 30

Broad Spectrum SPF 30
Sunscreen

Formulated with Thiamidol

Helps visibly reduce the look of persistent dark spots

DERMATOLGIST RECOMMENDED BRAND

OL

INGREDIENTS AND APPEARANCE

EUCERIN RADIANT TONE 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10356-395
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	8 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALCOHOL (UNII: 3K9958V90M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
GLYCYRRHIZA INFLATA ROOT EXTRACT (UNII: 1MV1Z7MKVQ)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
XANTHAN GUM (UNII: TTV12P4NEE)
ISOBUTYLAMIDO THIAZOLYL RESORCINOL (UNII: OH3UOW0EHH)
GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
DIBUTYL ADIPATE (UNII: F4K100DXP3)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
SILICA (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10356-395-05	1 in 1 CARTON	11/04/2024
1		50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 10356-395-02	7 g in 1 TUBE; Type 0: Not a Combination Product	11/04/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/04/2024

Labeler - Beiersdorf Inc (001177906)