B04 DIGESTION

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: B04 DIGESTION
Generic name: ALFALFA, ANTIMONIUM CRUDUM, AVENA SATIVA, BERBERIS VULGARIS, CAJUPUTUM, CARBO ANIMALIS, CARBO VEGETABILIS, CHELIDONIUM MAJUS, FEL TAURI, GENTIANA LUTEA, GLYCYRRHIZA GLABRA, ILLICIUM ANISATUM, INDOLUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, NUX VOMICA, PANCREATINUM, PEPSINUM, RAPHANUS SATIVUS, RHAMNUS PURSHIANA, SKATOLUM
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bad8bfa1-a882-65b1-e053-2995a90a02f7
SPL ID: 0e76a879-b2c8-dcc6-e063-6294a90ac60e
Version: 2
Effective date: 2024-01-08
Source export date: 2026-10-27
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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:59:49

Harmonized routes table
Harmonized routes
SUBLINGUAL

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 · 30 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		B04 DIGESTION	openfda.brand_name
generic name		ALFALFA, ANTIMONIUM CRUDUM, AVENA SATIVA, BERBERIS VULGARIS, CAJUPUTUM, CARBO ANIMALIS, CARBO VEGETABILIS, CHELIDONIUM MAJUS, FEL TAURI, GENTIANA LUTEA, GLYCYRRHIZA GLABRA, ILLICIUM ANISATUM, INDOLUM, KALI CARBONICUM, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, NUX VOMICA, PANCREATINUM, PEPSINUM, RAPHANUS SATIVUS, RHAMNUS PURSHIANA, SKATOLUM	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0204-1	openfda.package_ndc
ndc	product	63479-0204	openfda.product_ndc
ndc11	package	63479020401	derived:openfda.package_ndc
spl id		0e76a879-b2c8-dcc6-e063-6294a90ac60e	id
spl set id		bad8bfa1-a882-65b1-e053-2995a90a02f7	set_id
unii		2P3VWU3H10	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		2788Z9758H	openfda.unii
unii		269XH13919	openfda.unii
unii		DJO934BRBD	openfda.unii
unii		ET3651ZLOU	openfda.unii
unii		J3TO6BUQ37	openfda.unii
unii		XKC1657P78	openfda.unii
unii		8724FJW4M5	openfda.unii
unii		F79059A38U	openfda.unii
unii		S72O3284MS	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		4VBP01X99F	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		EM5RP35463	openfda.unii
unii		9W945B5H7R	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		GID333S43J	openfda.unii
unii		FQ3DRG0N5K	openfda.unii
unii		279O8I0433	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

If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if indigestion, bloating, stomach irritation/ache, flatulence, loss of appetite, or other symptoms do not improve within 7 days or are accompanied by fever.

Reported adverse events (FAERS/openFDA)#

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