FDA.reportPublic FDA data

DR H STABILIZER

Manufacturer
DIVERSIFIED MANUFACTURING CORP
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:13:11

Label at a glance#

ProductDR H STABILIZER
Active ingredientHYDROCORTISONE
Label structure9 sections

Indications and uses

PROVIDES HELP TO ITCHING ASSOCIATED WITH MINOR SKIN IRRITATION, ECZEMA, PSORIASIS, AND SEBORRHEIC DERMATITIS. OTHER USES OF THIS PRODUCT SHOULD BE UNDER THE ADVICE AND SUPERVISION OF A DOCTOR.

Dosage and administration

APPLY THIN LAYER TO AFFECTED AREA TWICE DAILY. DO NOT USE FOR MORE THAN 2 WEEKS WITHOUT PHYSICIAN SUPERVISION.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

HYDROCORTISONE 0.75%

PURPOSE

OTC - PURPOSE SECTION

ANTI-ITCH

USES

INDICATIONS & USAGE SECTION

PROVIDES HELP TO ITCHING ASSOCIATED WITH MINOR SKIN IRRITATION, ECZEMA, PSORIASIS, AND SEBORRHEIC DERMATITIS. OTHER USES OF THIS PRODUCT SHOULD BE UNDER THE ADVICE AND SUPERVISION OF A DOCTOR.

WARNINGS

WARNINGS SECTION

DISCONTINUE IF CONDITION IS NOT IMPROVING AND CONSULT YOUR PHYSICIAN.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY THIN LAYER TO AFFECTED AREA TWICE DAILY. DO NOT USE FOR MORE THAN 2 WEEKS WITHOUT PHYSICIAN SUPERVISION.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, PETROLATUM, GLYCERIN, STEARETH-2, DIMETHICONE, CETYL ALCOHOL, MAGNESIUM ALUMINUM SILICATE, BENZYL ALCOHOL, LAURETH-23, SULFUR, CARBOMER, METHYLPARABEN, PROPYLPARABEN, POTASSIUM SORBATE, XANTHAN GUM, SODIUM HYDROXIDE, FRAGRANCE.

OTHER INFORMATION

OTHER SAFETY INFORMATION

CONTAINS THE PURE ELEMENT SULFUR AND IS NOT RELATED TO "SULFA ALLERGY".

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DrH Stabilizer Lotion 2 oz. - 60 ml.jpgDrH Stabilizer Lotion 2 oz. - 60 ml.jpg

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62172-20362172-203-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM SORBATE1VPU26JZZ4IACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM HYDROXIDE55X04QC32IIACT
HYDROCORTISONEWI4X0X7BPJACTIB
WATER059QF0KO0RIACT
PETROLATUM4T6H12BN9UIACT
GLYCERINPDC6A3C0OXIACT
STEARETH-2V56DFE46J5IACT
DIMETHICONE92RU3N3Y1OIACT
CETYL ALCOHOL936JST6JCNIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
BENZYL ALCOHOLLKG8494WBHIACT
LAURETH-23N72LMW566GIACT
SULFUR70FD1KFU70IACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT

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
101c479c-7722-aef8-e063-6294a90a213e6a94cdb5-2aca-49a4-bbad-18d9925ea3582024-01-29WarningsExact identifier
spl set id: 6a94cdb5-2aca-49a4-bbad-18d9925ea358

Reported adverse events (FAERS/openFDA)#

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