SPL v1
SPL
SPL Set ID 3ba6a5ec-fda2-b2a6-e063-6294a90ac9b6
Route
TOPICAL
Published
Effective Date 2025-08-05
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Hydrocortisone (1 g)
Inactive Ingredients
Stearic Acid Diazolidinyl Urea Light Mineral Oil Propylparaben Water Glycerin Edetate Disodium Polyethylene Glycol, Unspecified Methylparaben Propylene Glycol Cetyl Alcohol Glyceryl Monostearate Trolamine

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2010-04-30

Description

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)


Medication Information

Warnings and Precautions

For external use only

Indications and Usage

Anti-itch ointment

Dosage and Administration

for the temporary relief of itching associated with minor skin irritations and rashes

other uses of this product should be only under the advice and supervision of a doctor

Dosage Forms and Strengths

2packs in 1pouch NDC (51662-1284-1)

Description

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

Section 50565-1

Keep out of the reach of children

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

Section 50566-9

Stop use and ask a doctor if

condition worsens

symptoms persist more than 7 days

condition clears up and occurs again within a few days

Section 50567-7

When using this product

avoid contact with eyes

do not begin use of any other hydrocortisone product unless you've consulted a doctor

Section 50570-1

Do not use

for the treatment of diaper rash. Consult a doctor

Section 51727-6

cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, stearic acid, trolamine, water

Section 51945-4

Section 55105-1

Anti-itch cream

Section 55106-9

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

Section 60561-8

clean the affected area

store at room temperature

do not use any opened or torn packets

you may report a serious adverse reaction to this product to 800-275-3433

Directions

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

children under 2 years; do not use, consult a doctor


Structured Label Content

Indications and Usage (34067-9)

Anti-itch ointment

Dosage and Administration (34068-7)

for the temporary relief of itching associated with minor skin irritations and rashes

other uses of this product should be only under the advice and supervision of a doctor

Dosage Forms and Strengths (34069-5)

2packs in 1pouch NDC (51662-1284-1)

Warnings and Precautions (34071-1)

For external use only

Section 50565-1 (50565-1)

Keep out of the reach of children

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

Section 50566-9 (50566-9)

Stop use and ask a doctor if

condition worsens

symptoms persist more than 7 days

condition clears up and occurs again within a few days

Section 50567-7 (50567-7)

When using this product

avoid contact with eyes

do not begin use of any other hydrocortisone product unless you've consulted a doctor

Section 50570-1 (50570-1)

Do not use

for the treatment of diaper rash. Consult a doctor

Section 51727-6 (51727-6)

cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, stearic acid, trolamine, water

Section 51945-4 (51945-4)

Section 55105-1 (55105-1)

Anti-itch cream

Section 55106-9 (55106-9)

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

Section 60561-8 (60561-8)

clean the affected area

store at room temperature

do not use any opened or torn packets

you may report a serious adverse reaction to this product to 800-275-3433

Directions (DIRECTIONS)

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

children under 2 years; do not use, consult a doctor


Advanced Ingredient Data


Raw Label Data

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