FDA.reportPublic FDA data

XZM CARE

Manufacturer
Lavior Inc.
Effective date
2021-03-16
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 22:48:56

Label at a glance#

ProductXZM CARE
Active ingredientOATMEAL
Label structure10 sections

Indications and uses

temporarily protects and helps relieve minor skin irritation and itching due to: rashes eczema

Dosage and administration

apply a thin layer 1 to 2 times daily, or as directed by a doctor for babies under 2 months of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Colloidal Oatmeal 1%......................Skin Protectant

Purpose:

OTC - PURPOSE SECTION

skin protectant

Uses:

INDICATIONS & USAGE SECTION

  • temporarily protects and helps relieve minor skin irritation and itching due to:
  • rashes
  • eczema

Warnings

WARNINGS SECTION

For external use only

When using this product

  • avoid contact with eyes

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.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply a thin layer 1 to 2 times daily, or as directed by a doctor
  • for babies under 2 months of age: ask a doctor

Other information

OTC - WHEN USING SECTION

  • for mild to moderate eczema
  • store at room temperature

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Inula Viscosa Flower/Leaf/Stem Extract, Xanthan Gum, Glyceryl Stearate Citrate, Aloe Barbadensis Leaf Juice, Propanediol-1,3, Cetyl Alcohol, Sodium Benzoate, Potassium Sorbate, Biosaccharide Gum-1, Tocopheryl Acetate (Vitamin E), Sodium Gluconate, Citric Acid.

Questions?

OTC - QUESTIONS SECTION

Call toll free 1-844-474-2552 or visit lavior.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

XZM CAREXZM CARE

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71521-67871521-678-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
OATMEAL8PI54V663YACTIB
SODIUM BENZOATEOJ245FE5EUIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
GLYCERINPDC6A3C0OXIACT
CETYL ALCOHOL936JST6JCNIACT
XANTHAN GUMTTV12P4NEEIACT
ALOE VERA LEAFZY81Z83H0XIACT
DITTRICHIA VISCOSA WHOLE3SYW69FH88IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM GLUCONATER6Q3791S76IACT
PROPANEDIOL5965N8W85TIACT
BIOSACCHARIDE GUM-1BB4PU4V09HIACT

Source Document#

Source XML

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
c5482950-ae59-7653-e053-2995a90ad5d75422fb7f-8dea-648b-e054-00144ff8d46c2021-06-21WarningsExact identifier
spl set id: 5422fb7f-8dea-648b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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