Poison Ivy Care

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: Poison Ivy Care
Generic name: CALENDULA OFFICIALS, STELLARIA MEDIA, ST. JOHNS WORT, ROSEMARY OIL, PLANTAGO MAJOR, COMMIPHORA MYRRHA, COMFREY LEAF, SALVIA OFFICINALIS, SUNFLOWER OIL
Manufacturer: Spry Life LLC
Product type: HUMAN OTC DRUG
SPL set ID: 480ee4ba-a92c-07ee-e054-00144ff8d46c
SPL ID: 4604c152-2f33-24fa-e063-6294a90a6f48
Version: 9
Effective date: 2025-12-15
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:37

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Poison Ivy Care	openfda.brand_name
generic name		CALENDULA OFFICIALS, STELLARIA MEDIA, ST. JOHNS WORT, ROSEMARY OIL, PLANTAGO MAJOR, COMMIPHORA MYRRHA, COMFREY LEAF, SALVIA OFFICINALIS, SUNFLOWER OIL	openfda.generic_name
manufacturer name		Spry Life LLC	openfda.manufacturer_name
ndc	package	70994-204-10	openfda.package_ndc
ndc	package	70994-204-09	openfda.package_ndc
ndc	package	70994-204-08	openfda.package_ndc
ndc	package	70994-204-01	openfda.package_ndc
ndc	package	70994-204-02	openfda.package_ndc
ndc	product	70994-204	openfda.product_ndc
ndc11	package	70994020401	derived:openfda.package_ndc
ndc11	package	70994020408	derived:openfda.package_ndc
ndc11	package	70994020409	derived:openfda.package_ndc
ndc11	package	70994020410	derived:openfda.package_ndc
ndc11	package	70994020402	derived:openfda.package_ndc
spl id		4604c152-2f33-24fa-e063-6294a90a6f48	id
spl set id		480ee4ba-a92c-07ee-e054-00144ff8d46c	set_id
unii		DG4F8T839X	openfda.unii
unii		UFH8805FKA	openfda.unii
unii		2H03479QVR	openfda.unii
unii		UU81N77RI7	openfda.unii
unii		YQR8R0SQEA	openfda.unii
unii		W2469WNO6U	openfda.unii
unii		P0M7O4Y7YD	openfda.unii
unii		M9C36LC10E	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 Section Warnings For external use only. ■ Do not use on ■ on deep wounds ■ animal bites ■ serious burns ■ 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 ■ When using this product keep out of eyes. Rinse with water to remove.

Reported adverse events (FAERS/openFDA)#

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