Rapidol

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Rapidol
Generic name: HYDROCORTISONE
Manufacturer: Pharmadel LLC
Product type: HUMAN OTC DRUG
SPL set ID: 19a1f1e2-bc6b-7153-e063-6294a90ab115
SPL ID: 491142b7-44da-7a1a-e063-6394a90a1942
Version: 6
Effective date: 2026-01-23
Source export date: 2026-10-12
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:11:38

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Rapidol	openfda.brand_name
generic name		HYDROCORTISONE	openfda.generic_name
manufacturer name		Pharmadel LLC	openfda.manufacturer_name
ndc	package	55758-420-03	openfda.package_ndc
ndc	package	55758-420-02	openfda.package_ndc
ndc	product	55758-420	openfda.product_ndc
ndc11	package	55758042002	derived:openfda.package_ndc
ndc11	package	55758042003	derived:openfda.package_ndc
rxcui		106258	openfda.rxcui
spl id		491142b7-44da-7a1a-e063-6394a90a1942	id
spl set id		19a1f1e2-bc6b-7153-e063-6294a90ab115	set_id
unii		WI4X0X7BPJ	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings FOR EXTERNAL USE ONLY. Avoid contact with the eyes. Do not use for treatment of diaper rash. Consult a doctor if you have a vaginal discharge. Consult a doctor. with any other hydrocortisone product unless you have consulted a doctor When using this product for external anal itching: Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days and occur again within a few days If pregnant or breastfeeding, ask a doctor before use. KEEP OUT OF REACH OF CHILDREN If accidental ingestion, seek medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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