FDA.reportPublic FDA data

D-Care

Manufacturer
Lavior Inc.
Effective date
2020-12-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:04:47

Label at a glance#

ProductD-Care
Active ingredientALLANTOIN
Label structure13 sections

Indications and uses

helps prevent and relieve dry, chafed, chapped, or cracked skin temporarily protects minor cuts, scrapes, and burns helps protect from the drying effects of wind and cold weather

Dosage and administration

apply a thin layer 1 to 2 times daily, or as directed by a doctor

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%

OTC - PURPOSE SECTION

Skin Protectant

Uses:

INDICATIONS & USAGE SECTION

  • helps prevent and relieve dry, chafed, chapped, or cracked skin
  • temporarily protects minor cuts, scrapes, and burns
  • helps protect from the drying effects of wind and cold weather

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

OTC - DO NOT USE SECTION

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply a thin layer 1 to 2 times daily, or as directed by a doctor

Other information

OTC - WHEN USING SECTION

  • store at room temperature

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Inula Viscosa Flower/Leaf/Stem Extract, Xanthan Gum, Sodium Benzoate, Potassium Sorbate, Aloe Barbadensis Leaf Juice, Citric Acid, Tocopheryl Acetate (Vitamin E), Sodium Hyaluronate

OTC - QUESTIONS SECTION

Questions? Call toll free 1844-474-2552 or visit www.lavior.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

D-CARE OTCD-CARE OTC

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71521-77771521-777-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZACTIB
SODIUM BENZOATEOJ245FE5EUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
DITTRICHIA VISCOSA WHOLE3SYW69FH88IACT
HYALURONATE SODIUMYSE9PPT4THIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
XANTHAN GUMTTV12P4NEEIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
MALTODEXTRIN7CVR7L4A2DIACT
SODIUM GLUCONATER6Q3791S76IACT

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
c3f88331-8d6f-2786-e053-2995a90ac99555b1f3b7-7ccb-3b2b-e054-00144ff88e882021-06-04WarningsExact identifier
spl set id: 55b1f3b7-7ccb-3b2b-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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