QUATRIDERM CREME NF

Manufacturer
OPMX LLC
Effective date
2020-10-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:10:12

Label at a glance#

ProductQUATRIDERM CREME NF
Active ingredientHYDROCORTISONE
Label structure9 sections

Indications and uses

FOR THE TEMPORARY RELIEF OF ITCHING ASSOCIATED WITH MINOR SKIN IRRITATIONS, INFLAMMATION, AND RASHES DUE TO:     ECZEMA     SEBORRHEIC DERMATITIS     PSORIASIS        INSECT BITES     POISON IVY, POISON OAK, AND POISON SUMAC     COSMETICS     JEWELRY     DETERGENTS     SOAPS TEMPORARILY RELIEVES EXTERNAL ANAL AND GENITAL ITCHING OTHER USES OF THIS PRODUC SHOULD BE ONLY UNDER THE ADVICE AND SUPERVISION OF A DOCTOR

Dosage and administration

ADULTS AND CHILDREN 2 YEARS AND OVER: APPLY TO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY. CHILDREN UNDER 2 YEARS: ASK A DOCTOR FOR EXTERNAL ANAL ITCHING IN ADULTS:     WHEN PRACTICAL, CLEANSE THE AFFECTED AREA WITH MILD SOAP AND WARM WATER AND RINSE THOROUGHLY, OR BY PATTING OR BLOTTING WITH AN APPROPRIATE CLEANSING PAD     GENTLY DRY BY PATTING OR BLOTTING WITH TOILET TISSUE OR A SOFT CLOTH BEFORE APPLYING. ...

Storage and handling

STORE AT 20°C TO 25°C (68°F TO 77°F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

HYDROCORTISONE USP 1%

PURPOSE

OTC - PURPOSE SECTION

ANTI-ITCH

USES

INDICATIONS & USAGE SECTION

  • FOR THE TEMPORARY RELIEF OF ITCHING ASSOCIATED WITH MINOR SKIN IRRITATIONS, INFLAMMATION, AND RASHES DUE TO:
  •     ECZEMA
  •     SEBORRHEIC DERMATITIS
  •     PSORIASIS   
  •     INSECT BITES
  •     POISON IVY, POISON OAK, AND POISON SUMAC
  •     COSMETICS
  •     JEWELRY
  •     DETERGENTS
  •     SOAPS
  • TEMPORARILY RELIEVES EXTERNAL ANAL AND GENITAL ITCHING
  • OTHER USES OF THIS PRODUC SHOULD BE ONLY UNDER THE ADVICE AND SUPERVISION OF A DOCTOR

WARNINGS

WARNINGS SECTION

For external use only.

DO NOT USE

  • FOR THE TREATMENT OF DIAPER RASH. ASK A DOCTOR.
  • FOR EXTERNAL GENITAL ITCHING IF YOU HAVE A VAGINAL DISCGARGE. ASK A DOCTOR.
  • FOR EXTERNAL ANAL ITCHING IF RECTAL BLEEDING OCCURS. CONSULT A DOCTOR PROMPTLY.

WHEN USING THIS PRODUCT

  • DO NOT GET INTO THE EYES
  • FOR EXTERNAL ANAL ITCHING, DO NOT USE MORE THAN DIRECTED UNLESS TOLD TO DO SO BY A DOCTOR
  • DO NOT PUT INTO THE RECTUM BY USING FINGERS OR ANY MECHANICAL DEVICE OR APPLICATOR

STOP USE AND ASK A DOCTOR IF

  • CONDITION GETS WORSE, OR IF SYMPTOMS LAST FOR MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS. DO NOT BEGIN USE OF ANY OTHER HYDROQUINONE PRODUCT.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed get medical help or contact Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • ADULTS AND CHILDREN 2 YEARS AND OVER: APPLY TO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY.
  • CHILDREN UNDER 2 YEARS: ASK A DOCTOR
  • FOR EXTERNAL ANAL ITCHING IN ADULTS:
  •     WHEN PRACTICAL, CLEANSE THE AFFECTED AREA WITH MILD SOAP AND WARM WATER AND RINSE THOROUGHLY, OR BY PATTING OR BLOTTING WITH AN APPROPRIATE CLEANSING PAD
  •     GENTLY DRY BY PATTING OR BLOTTING WITH TOILET TISSUE OR A SOFT CLOTH BEFORE APPLYING.
  • FOR EXTERNAL ANAL ITCHING IN CHILDREN UNDER 12 YEARS: ASK A DOCTOR.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • STORE AT 20°C TO 25°C (68°F TO 77°F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ALOE VERA LEAF EXTRACT, CETOSTEARYL ALCOHOL, GLYCERYL MONOSTEARATE SE, METHYLISOTHIAZOLINONE, PROPYLENE GLYCOL, PURIFIED WATER, STEARIC ACID, TRIETHANOLAMINE, WHITE SOFT PARAFFIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Quatriderm_2oz01b UC_Quatriderm_2oz

01b UC_Quatriderm_2oz_DF Box01b UC_Quatriderm_2oz_DF Box

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69729-10269729-102-12, 69729-102-52
61040-219

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
ced79192-0b52-48c1-9fc5-ac61c39a6b4518447735-d022-4dfa-95db-9b508786bb602020-11-22WarningsExact identifier
spl set id: 18447735-d022-4dfa-95db-9b508786bb60

Reported adverse events (FAERS/openFDA)#

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