Indications and uses
for the temporary relief of itching associated with minor irritations and rashes other uses of this product should be only under the advice and superivision of a doctor.
Hydrocortisone
- Manufacturer
- Nantong Health & Beyond Hygienic Products Inc.
- Effective date
- 2024-08-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 00:17:04
Label at a glance#
ProductHydrocortisone
Active ingredientHYDROCORTISONE
Label structure6 sections
Dosage and administration
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 of age: do not use.
Label contents#
Full prescribing information#
Active ingredient
Hydrocortisone 1%
Purpose
Anti-itch
Uses
- for the temporary relief of itching associated with minor irritations and rashes
- other uses of this product should be only under the advice and superivision of a doctor.
Warnings
For external use only.
Avoid contact with the eyes.
Do not use
for the treatment of diaper rash. Consult a doctor.
Do not use, consult a doctor
if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, stop use of this product and do not begin use of any other hydrocortisone product unless you have consulted a doctor.
Do not use if the packaging is broken
Keep out of reach of children.
If swallowed contact a Poison Control Center right away.
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 of age: do not use.
Inactive ingredients
Cetearyl alcohol, Ceteareth-20, Ethylhexylglycerin, Glycerin, Glycerol fatty acid ester, Mineral Oil, Petrolatum, Phenoxyethanol, Water
Package Labeling:
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 106258 | hydrocortisone 1 % Topical Cream | PSN | 3 |
| 106258 | hydrocortisone 10 MG/ML Topical Cream | SCD | 3 |
| 106258 | hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream | SY | 3 |
| 106258 | hydrocortisone 1 % Topical Cream | SY | 3 |
| 106258 | hydrocortisone 1 GM per 100 GM Topical Cream | SY | 3 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| HYDROCORTISONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43473-049-01 | Hydrocortisone | 0.9 g in 1 PACKET | CREAM | 0.9 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hydrocortisone
- CETOSTEARYL ALCOHOL
- POLYOXYL 20 CETOSTEARYL ETHER
- ETHYLHEXYLGLYCERIN
- GLYCERIN
- MINERAL OIL
- PETROLATUM
- PHENOXYETHANOL
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43473-049 | 43473-049-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CETOSTEARYL ALCOHOL | 2DMT128M1S | IACT |
| POLYOXYL 20 CETOSTEARYL ETHER | YRC528SWUY | IACT |
| ETHYLHEXYLGLYCERIN | 147D247K3P | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| MINERAL OIL | T5L8T28FGP | IACT |
| PETROLATUM | 4T6H12BN9U | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| WATER | 059QF0KO0R | IACT |
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Hydrocortisone | HYDROCORTISONE | Nantong Health & Beyond Hygienic Products Inc. | fbbbcc67-b46d-d41a-e053-6294a90aa55d | 2024-08-08 | Warnings | 43473-049-01 43473-049 43473004901 1f390f4e-6459-89ef-e063-6294a90a33ed fbbbcc67-b46d-d41a-e053-6294a90aa55d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.