OTC - ACTIVE INGREDIENT SECTION
Hydrocortisone 1%
Hydrocortisone 1%
Antipruritic (Anti-itch)
Relieves itches and rashes due to:
Eczema
Psoriasis
Seborrheic dermatitis
Poison ivy
Poison oak
Poison sumac
Insect bites
External anal itching
Soaps
Detergents
Cosmetics
Jewelry
Temporary relief of external anal and genital itching.
Other use of the product should only be under the advice and supervision of a doctor.
For external use only
Do not use:
In the eyes
For diaper rash
If you have vaginal discharge
More than the recommended dosage
Ask doctor before use:
If you are pregnant or breast feeding
Stop use and ask a doctor if:
Condition worsens, or is symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor.
When using this product:
Do not put this product into rectum by using fingers or any mechanical device or applicator.
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away
Adults and children over 2 years of age - Apply to affected area not more than 3-4 times per day.
Children under 2 years of age - Do not use. Consult a doctor.
For external anal itching Adults - When practical cleanse the affcted area with mild soap and water and rinse thoroughly. Gently dry patting with bathroom tissue or soft cloth before applying. Apply to affected area not more than 3-4 times per day. Children under 12 years of age: consult a doctor.
store between 20ºC and 25ºC (68ºFk and 77ºF)
avoid excessive heat and humidity
Cetomacrogol 1000, Cetostearyl alcohol, Chlorocresol, Disodium EDTA, Liquid paraffin, Propylene glycol, Purified water, Sodium metabisulphite, White soft paraffin.
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72189-276-28 | GM - Gram | 72189-276 | 299cf256-53a4-4510-8368-2b054466caec | 1 | 2021-11-09 |
| 70512-101-30 | GM - Gram | 70512-101 | 63cc083c-6e85-434c-9785-501ae92e4f12 | 1 | 2020-08-06 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72189-276 | 72189-276-28 |
| 70512-101 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PETROLATUM | 4T6H12BN9U | IACT |
| MINERAL OIL | T5L8T28FGP | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| CHLOROCRESOL | 36W53O7109 | IACT |
| CETOSTEARYL ALCOHOL | 2DMT128M1S | IACT |
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
| WATER | 059QF0KO0R | IACT |
| CETETH-20 | I835H2IHHX | IACT |
| DISODIUM EDTA-COPPER | 6V475AX06U | IACT |
| SODIUM METABISULFITE | 4VON5FNS3C | IACT |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 074aa01c-4b42-5382-e063-6394a90abefb | cc82086b-3034-1805-e053-2a95a90af0bd | 2023-10-09 | Warnings | cc82086b-3034-1805-e053-2a95a90af0bd |
Adverse event summaries are temporarily unavailable. Other product information remains available.