EUCERIN SKIN CALMING ITCH RELIEF TREATMENT- menthol lotion

Eucerin Skin Calming Itch Relief Treatment by

Drug Labeling and Warnings

Eucerin Skin Calming Itch Relief Treatment by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 0.1%

PURPOSE

External analgesic lotion

INDICATIONS & USAGE

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

WARNINGS

For external use only.

WHEN USING

When using this product avoid contact with eyes.

STOP USE

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

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.

QUESTIONS

Questions or comments 1 800 227 4703

INACTIVE INGREDIENT

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, PEG-40 Castor Oil, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Cetearyl Sulfate, Sodium Citrate, Polyglyceryl-3 Methyl Glucose Distearate, 1,2-Hexanediol, Piroctone Olamine, Potassium Sorbate, Citric Acid

DOSAGE & ADMINISTRATION

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

PRINCIPAL DISPLAY PANEL

Eucerin

Skin Calming Itch Relief Treatment

Immediately relieves and calms dry, itchy skin

Cooling menthol enriched

Fragrance Free

External Analgesic Lotion

INGREDIENTS AND APPEARANCE

EUCERIN SKIN CALMING ITCH RELIEF TREATMENT 
menthol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10356-357
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
CETYL ALCOHOL (UNII: 936JST6JCN)
OATMEAL (UNII: 8PI54V663Y)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
OENOTHERA BIENNIS (UNII: 76UI55V071)
POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
OCTYLDODECANOL (UNII: 461N1O614Y)
PIROCTONE OLAMINE (UNII: A4V5C6R9FB)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10356-357-20	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/30/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/30/2018

Labeler - Beiersdorf Inc (001177906)