ALDICOM

Manufacturer: NAME
Effective date: 2021-12-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:45:57

Label at a glance#

ProductALDICOM

Active ingredientLACTOBACILLUS PLANTARUM

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ALDICOM A-HAT, lactobacillus

INACTIVE INGREDIENT SECTION

fryctiikugisaccgarudem sugar fed honey, glucomannan, pueraria montana var. lobata extract

OTC - PURPOSE SECTION

Alcohol decomposition

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Take 1ea before and after drinking

WARNINGS SECTION

Do not take in excess of the specified dose

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73392-0002-1	2023-01-30	C162847	48780-1	f386c649-d80b-0266-e053-dadaa90a7c1a	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73392-0002-1	ALDICOM	75 g in 1 PACKAGE	LIQUID	75		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73392-0002	ALDICOM (ALDICOM A-HAT COMPLEX) LIQUID [NAME]	2	Legacy NDC, 1 package rows	20211228_9470189b-0580-5419-e053-2995a90a73fe.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

ALDICOM
Aldicom A-HAT Complex
HOVENIA DULCIS WHOLE
LACTOBACILLUS PLANTARUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73392-0002	73392-0002-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HOVENIA DULCIS WHOLE	1DM83BAP2N	IACT
LACTOBACILLUS PLANTARUM	QFC21096ON	ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d41c5905-62e0-83b6-e053-2995a90a53d0			9470189b-0580-5419-e053-2995a90a73fe	2021-12-27	Warnings	Exact identifier spl id: d41c5905-62e0-83b6-e053-2995a90a53d0 spl set id: 9470189b-0580-5419-e053-2995a90a73fe

Reported adverse events (FAERS/openFDA)#

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