Derma Pain

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: Derma Pain
Generic name: CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII)
Manufacturer: Liddell Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e02a5e99-aa27-4276-a785-7b5328d89fdc
SPL ID: f378a799-7c5f-45bf-a78b-1f9617f30121
Version: 2
Effective date: 2024-11-04
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:35

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Derma Pain	openfda.brand_name
generic name		CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII)	openfda.generic_name
manufacturer name		Liddell Laboratories, Inc.	openfda.manufacturer_name
ndc	package	50845-0280-1	openfda.package_ndc
ndc	product	50845-0280	openfda.product_ndc
ndc11	package	50845028001	derived:openfda.package_ndc
spl id		f378a799-7c5f-45bf-a78b-1f9617f30121	id
spl set id		e02a5e99-aa27-4276-a785-7b5328d89fdc	set_id
unii		2H1576D5WG	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		W2469WNO6U	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		0HK2GZK66E	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. If symptoms persist for more than 7 days, consult a doctor. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away. Do not get into eyes Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Reported adverse events (FAERS/openFDA)#

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