PTS/Stress Remedy

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: PTS/Stress Remedy
Generic name: KALI PHOSPHORICUM, AMBRA GRISEA, CACAO, PHOSPHORICUM ACIDUM, ARNICA MONTANA, CALCAREA CARBONICA, CEREBRUM SUIS, GLANDULA SUPRARENALIS SUIS, LITHIUM CARBONICUM, ACONITUM NAPELLUS, ARGEMONE MEXICANA, ARSENICUM ALBUM, CICUTA VIROSA, HYOSCYAMUS NIGER, IGNATIA TIGRINUM, NATRUM MURIATICUM, TARENTULA HISPANICA, STRAMONIUM, BUTHUS AUSTRALIS
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 05341147-789a-4844-9412-6a3044e5eb18
SPL ID: 57eaf84a-12fd-4a9d-b4ff-68e78f5ca2b9
Version: 2
Effective date: 2024-03-04
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:12:30

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		PTS/Stress Remedy	openfda.brand_name
generic name		KALI PHOSPHORICUM, AMBRA GRISEA, CACAO, PHOSPHORICUM ACIDUM, ARNICA MONTANA, CALCAREA CARBONICA, CEREBRUM SUIS, GLANDULA SUPRARENALIS SUIS, LITHIUM CARBONICUM, ACONITUM NAPELLUS, ARGEMONE MEXICANA, ARSENICUM ALBUM, CICUTA VIROSA, HYOSCYAMUS NIGER, IGNATIA TIGRINUM, NATRUM MURIATICUM, TARENTULA HISPANICA, STRAMONIUM, BUTHUS AUSTRALIS	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1322-1	openfda.package_ndc
ndc	product	43742-1322	openfda.product_ndc
ndc11	package	43742132201	derived:openfda.package_ndc
spl id		57eaf84a-12fd-4a9d-b4ff-68e78f5ca2b9	id
spl set id		05341147-789a-4844-9412-6a3044e5eb18	set_id
unii		4GB5DQR532	openfda.unii
unii		CI71S98N1Z	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		2E32821G6I	openfda.unii
unii		4WRK2153H3	openfda.unii
unii		X67Z2963PI	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		D9108TZ9KG	openfda.unii
unii		XTC0D02P6C	openfda.unii
unii		86M454L2TT	openfda.unii
unii		6X68976407	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		G6W4F0V8Z3	openfda.unii
unii		25IMQ489AW	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		2BMD2GNA4V	openfda.unii
unii		YEA9P21S8N	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: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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