Itch relief Cream

Manufacturer
Cintas Corporation | ULTRAtab Laboratories, Inc. | Ultra Seal Corporation
Effective date
2021-01-11
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:57:09

Label at a glance#

ProductItch relief Cream
Active ingredientHYDROCORTISONE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: HYDROCORTISONE 1%Cream.

OTC - PURPOSE SECTION

Itch Relief Cream

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Benzoic Acid, Chlorphenesin, Citric Acid, Glycerin,Glycerol Monostearate, Methyl Paraben, Mineral Oil,Petrolatum, Phenoxyethanol,Polysorbate 80,Purified Water, Titanium Dioxide,Trisodium Citrate

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

USES: For the temporary relief of itching associated with minor, skin irritations and rashes due to eczema, insect bites, poison ivy/oak/sumac, soaps, detergents,cosmetics and jewelry

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults and children 2years of age and older: apply to affected area and not more than 3 to4 times daity. Children under 2: do not use, consult a doctor.

WARNINGS SECTION

WARNINGS: For external use only. Avoid contact with eyes. Discontinue use If conditions persist more than 7 days and consult a physician. Do not use on children under 2 years except under the advice and supervision of a physician. Do not use with any other hydrocortisone product unless you have consulted a doctor. Other uses or this product should be only under the advise or supervision of a doctor.

OTHER SAFETY INFORMATION

Store at room temperature (do not freeze).

PACKET NOT FOR INDIVIDUAL SALE

Tamper evident: Do not use if package is torn or cut.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cintas HC cream 2016Cintas HC cream 2016

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
42961-37042961-370-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
83a3c1a5-ea24-489b-952e-01ab3565143e65817c17-5ecb-4f2f-b588-4354329c19422022-12-29WarningsExact identifier
spl set id: 65817c17-5ecb-4f2f-b588-4354329c1942

Reported adverse events (FAERS/openFDA)#

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