Schuessler Tissue Salts Comb 12 General Tonic

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: Schuessler Tissue Salts Comb 12 General Tonic
Generic name: CALCAREA FLUORICA,CALCAREA PHOSPHORICA,CALCAREA SULPHURICA,FERRUM PHOSPHORICUM,KALI PHOSPHORICUM,KALI MURIATICUM,KALI SULPHURICUM,MAGNESIA PHOSPHORICA,NATRUM MURIATICUM,NATRUM PHOSPHORICUM,NATRUM SULPHURICUM,SILICEA
Manufacturer: Martin & Pleasance Pty Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 9083a01b-2fbe-4e04-9eec-bf4f65950ec7
SPL ID: 3e5f0fc5-ee2b-09fd-e063-6394a90addba
Version: 1
Effective date: 2025-09-09
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:58

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Schuessler Tissue Salts Comb 12 General Tonic	openfda.brand_name
generic name		CALCAREA FLUORICA,CALCAREA PHOSPHORICA,CALCAREA SULPHURICA,FERRUM PHOSPHORICUM,KALI PHOSPHORICUM,KALI MURIATICUM,KALI SULPHURICUM,MAGNESIA PHOSPHORICA,NATRUM MURIATICUM,NATRUM PHOSPHORICUM,NATRUM SULPHURICUM,SILICEA	openfda.generic_name
manufacturer name		Martin & Pleasance Pty Ltd	openfda.manufacturer_name
ndc	package	84999-029-01	openfda.package_ndc
ndc	product	84999-029	openfda.product_ndc
ndc11	package	84999002901	derived:openfda.package_ndc
spl id		3e5f0fc5-ee2b-09fd-e063-6394a90addba	id
spl set id		9083a01b-2fbe-4e04-9eec-bf4f65950ec7	set_id
unii		22ADO53M6F	openfda.unii
unii		CI71S98N1Z	openfda.unii
unii		O3B55K4YKI	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		4846Q921YM	openfda.unii
unii		1K573LC5TV	openfda.unii
unii		660YQ98I10	openfda.unii
unii		D07L04MRWI	openfda.unii
unii		A1Y870209Z	openfda.unii
unii		36KCS0R750	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 Ask a doctor before use if you have : Symptoms persist for more than 7 days or worsen New symptoms occur Redness, swelling, or inflammation is present Pain gets worse or lasts more than 7 days. If pregnant or breastfeeding , ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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