FDA.reportPublic FDA data

Eucerin Skin Calming

Manufacturer
Beiersdorf Inc
Effective date
2019-12-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:47:28

Label at a glance#

ProductEucerin Skin Calming
Active ingredientMENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.1%

OTC - PURPOSE SECTION

External analgesic lotion

INDICATIONS & USAGE SECTION

Use for the temporary relief of itching associated with minor skin irritations.

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days
  • irritation occurs

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.

OTC - QUESTIONS SECTION

Questions or comments ? 1-800-227-4703

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Water, Glycerin, Octyldodecanol, Caprylic/Capric Triglyceride, Isopropyl Stearate, Myristyl Myristate, Cetyl Alcohol, Colloidal Oatmeal, Cetearyl Alcohol, Dimethicone, Glyceryl Stearate SE, Oenothera Biennis (Evening Primrose) Oil, Benzyl Alcohol, Phenoxyethanol, DMDM Hydantoin, PEG-40 Castor Oil, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Cetearyl Sulfate, Sodium Citrate, Polyglyceryl-3 Methyl Glucose Distearate, Potassium Sorbate, Citric Acid

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 8 years of age and older

  • apply to affected area not more than 3 to 4 times daily

Children under 8 years of age
consult a doctor

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Eucerin

Skin Calming

Cooling Menthol Enriched

Calms and Soothes dry, itchy skin

External Analgesic Lotion

Fragrance Free

Dry, Itchy Skin

Deermatological Skincare

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Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10356-35610356-356-20, 10356-356-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
OCTYLDODECANOL461N1O614YIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ISOPROPYL STEARATE43253ZW1MZIACT
MYRISTYL MYRISTATE4042ZC00DYIACT
CETYL ALCOHOL936JST6JCNIACT
OATMEAL8PI54V663YIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
OENOTHERA BIENNIS76UI55V071IACT
POLYOXYL 40 CASTOR OIL4ERD2076EFIACT
CAPRYLYL GLYCOL00YIU5438UIACT
SODIUM CETOSTEARYL SULFATE7ZBS06BH4BIACT
SODIUM CITRATE1Q73Q2JULRIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZYL ALCOHOLLKG8494WBHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DMDM HYDANTOINBYR0546TOWIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML · Source PDF

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
9aee2dcd-ca04-7ac0-e053-2995a90ae8d143082dcb-3ef7-6857-e054-00144ff88e882019-12-30WarningsExact identifier
spl id: 9aee2dcd-ca04-7ac0-e053-2995a90ae8d1
spl set id: 43082dcb-3ef7-6857-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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