Dr. Talbots Tummy Ache Relief

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: Dr. Talbots Tummy Ache Relief
Generic name: CALENDULA OFFICINALIS, CARBO VEGETABILIS, CHAMOMILLA, FOENICULUM VULGARE, LYCOPODIUM, NUX MOSCHATA, ZINGIBER OFFICINALE, KALI MURIATICUM, MAGNESIA PHOSPHORICA, NATRUM PHOSPHORICUM
Manufacturer: Talbot's Pharmaceuticals Family Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 91c1e0ae-9999-0ae2-e053-2995a90a2d71
SPL ID: cda11fa8-ab3d-bd89-e053-2a95a90a8c0e
Version: 3
Effective date: 2021-10-05
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:18

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		Dr. Talbots Tummy Ache Relief	openfda.brand_name
generic name		CALENDULA OFFICINALIS, CARBO VEGETABILIS, CHAMOMILLA, FOENICULUM VULGARE, LYCOPODIUM, NUX MOSCHATA, ZINGIBER OFFICINALE, KALI MURIATICUM, MAGNESIA PHOSPHORICA, NATRUM PHOSPHORICUM	openfda.generic_name
manufacturer name		Talbot's Pharmaceuticals Family Products, LLC	openfda.manufacturer_name
ndc	package	70797-311-04	openfda.package_ndc
ndc	package	70797-311-01	openfda.package_ndc
ndc	product	70797-311	openfda.product_ndc
ndc11	package	70797031101	derived:openfda.package_ndc
ndc11	package	70797031104	derived:openfda.package_ndc
spl id		cda11fa8-ab3d-bd89-e053-2a95a90a8c0e	id
spl set id		91c1e0ae-9999-0ae2-e053-2995a90a2d71	set_id
unii		2P3VWU3H10	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		AEE24M3MQ9	openfda.unii
unii		G3QC02NIE6	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		660YQ98I10	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		C5529G5JPQ	openfda.unii
unii		70WT22SF4B	openfda.unii
unii		C88X29Y479	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 Stop use and ask doctor if: fever develops diarrhea lasts more than 2 days other symptoms persist for more than 7 days or worsen Ask a doctor before use if you are taking a prescription drug or have a serious medical condition. Please consult your physician immediately for a worsening condition. warnings

Reported adverse events (FAERS/openFDA)#

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