Appetite Control

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: Appetite Control
Generic name: ADENOSINUM TRIPHOSPHORICUM DINATRUM, ADRENAL CORTEX (SUIS), BACOPA SPECIOSA, CHININUM SULPHURICUM, CINA, DOPAMINE HYDROCHLORIDE, EQUOL, GAMBOGIA, IODIUM, LYCOPODIUM CLAVATUM, MORGAN GAERTNER, OXYTOCIN, PANTOTHENIC ACID, PHOSPHORUS, RHODIOLA, SEROTONIN (HYDROCHLORIDE), STOMACH (SUIS), THYROIDINUM (SUIS)
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6d02621f-7983-4317-8a09-b11bf7ac7b09
SPL ID: be07c45e-1f9e-43ed-8d52-c2eddf5fb3bc
Version: 3
Effective date: 2024-03-05
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 06:18:06

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Appetite Control	openfda.brand_name
generic name		ADENOSINUM TRIPHOSPHORICUM DINATRUM, ADRENAL CORTEX (SUIS), BACOPA SPECIOSA, CHININUM SULPHURICUM, CINA, DOPAMINE HYDROCHLORIDE, EQUOL, GAMBOGIA, IODIUM, LYCOPODIUM CLAVATUM, MORGAN GAERTNER, OXYTOCIN, PANTOTHENIC ACID, PHOSPHORUS, RHODIOLA, SEROTONIN (HYDROCHLORIDE), STOMACH (SUIS), THYROIDINUM (SUIS)	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2094-1	openfda.package_ndc
ndc	product	43742-2094	openfda.product_ndc
ndc11	package	43742209401	derived:openfda.package_ndc
spl id		be07c45e-1f9e-43ed-8d52-c2eddf5fb3bc	id
spl set id		6d02621f-7983-4317-8a09-b11bf7ac7b09	set_id
unii		27YLU75U4W	openfda.unii
unii		28M1820ACT	openfda.unii
unii		T0920P9Z9A	openfda.unii
unii		6RV024OAUQ	openfda.unii
unii		19F5HK2737	openfda.unii
unii		GKN429M9VS	openfda.unii
unii		5L51B4DR1G	openfda.unii
unii		3S5ITS5ULN	openfda.unii
unii		7556HJ7587	openfda.unii
unii		7L3E358N9L	openfda.unii
unii		9679TC07X4	openfda.unii
unii		1JQS135EYN	openfda.unii
unii		Y3V16D4PV4	openfda.unii
unii		2T6D2HPX7Q	openfda.unii
unii		0G750PYD4W	openfda.unii
unii		Y04287JMZN	openfda.unii
unii		C88X29Y479	openfda.unii
unii		KF7Z0E0Q2B	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 breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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