PULSATILLA

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: PULSATILLA
Generic name: PULSATILLA
Manufacturer: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Product type: HUMAN OTC DRUG
SPL set ID: d8607ae4-3fbb-4c0a-9b3b-d9b6ad671c73
SPL ID: ca3d8643-bdbe-56d7-e053-2a95a90a6e8b
Version: 2
Effective date: 2021-09-02
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:12:16

Harmonized routes table
Harmonized routes
ORAL

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		PULSATILLA	openfda.brand_name
generic name		PULSATILLA	openfda.generic_name
manufacturer name		Rxhomeo Private Limited d.b.a. Rxhomeo, Inc	openfda.manufacturer_name
ndc	package	15631-0357-2	openfda.package_ndc
ndc	package	15631-0357-6	openfda.package_ndc
ndc	package	15631-0357-4	openfda.package_ndc
ndc	package	15631-0357-5	openfda.package_ndc
ndc	package	15631-0357-1	openfda.package_ndc
ndc	package	15631-0357-0	openfda.package_ndc
ndc	package	15631-0357-7	openfda.package_ndc
ndc	package	15631-0357-3	openfda.package_ndc
ndc	product	15631-0357	openfda.product_ndc
ndc11	package	15631035707	derived:openfda.package_ndc
ndc11	package	15631035706	derived:openfda.package_ndc
ndc11	package	15631035702	derived:openfda.package_ndc
ndc11	package	15631035704	derived:openfda.package_ndc
ndc11	package	15631035703	derived:openfda.package_ndc
ndc11	package	15631035700	derived:openfda.package_ndc
ndc11	package	15631035705	derived:openfda.package_ndc
ndc11	package	15631035701	derived:openfda.package_ndc
spl id		ca3d8643-bdbe-56d7-e053-2a95a90a6e8b	id
spl set id		d8607ae4-3fbb-4c0a-9b3b-d9b6ad671c73	set_id
unii		I76KB35JEV	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 This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children

Reported adverse events (FAERS/openFDA)#

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