SunBurnt Advanced After-Sun

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: SunBurnt Advanced After-Sun
Generic name: CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA
Manufacturer: Welmedix LLC
Product type: HUMAN OTC DRUG
SPL set ID: dcb2fd62-df8e-4a26-b7ed-274caefeeb76
SPL ID: 3d715022-70be-44aa-bfa3-f37823e35421
Version: 4
Effective date: 2018-03-20
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:29:53

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		SunBurnt Advanced After-Sun	openfda.brand_name
generic name		CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA	openfda.generic_name
manufacturer name		Welmedix LLC	openfda.manufacturer_name
ndc	package	24330-210-21	openfda.package_ndc
ndc	package	24330-210-06	openfda.package_ndc
ndc	package	24330-210-01	openfda.package_ndc
ndc	package	24330-210-03	openfda.package_ndc
ndc	product	24330-210	openfda.product_ndc
ndc11	package	24330021006	derived:openfda.package_ndc
ndc11	package	24330021003	derived:openfda.package_ndc
ndc11	package	24330021001	derived:openfda.package_ndc
ndc11	package	24330021021	derived:openfda.package_ndc
spl id		3d715022-70be-44aa-bfa3-f37823e35421	id
spl set id		dcb2fd62-df8e-4a26-b7ed-274caefeeb76	set_id
unii		3Q034RO3BT	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		P0M7O4Y7YD	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 Do not use on severe sunburn on broken skin if you have a rash if you have an allergy or hypersensitivity to any ingredients When using this product avoid contact with eyes or mucous membranes Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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