GI Clear P

Product NDC: 44911-0611
Requested package NDC: 44911-0611-1
11-digit product format: 449110611
Labeler code: 44911
Product ID: 44911-0611_787bc0d6-e847-4983-b9eb-e1bbba4c7c9c
Type: HUMAN OTC DRUG
Nonproprietary name: Arsenicum Album, Baptisia Tinctoria, Lachesis Mutus, Pulsatilla (Pratensis), Rhus Tox
Dosage form: LIQUID
Route: ORAL
Labeler: Energique, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2021-06-21
Marketing end: 2028-12-12
Substance: ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; LACHESIS MUTA VENOM; PULSATILLA PRATENSIS WHOLE; TOXICODENDRON PUBESCENS LEAF
Active strength: 10; 10; 10; 10; 10 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag: No
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: GI Clear P

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ARSENIC TRIOXIDE	10 [hp_X]/mL
BAPTISIA TINCTORIA ROOT	10 [hp_X]/mL
LACHESIS MUTA VENOM	10 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE	10 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF	10 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
S7V92P67HO	Internal UNII lookup
5EF0HWI5WU	Internal UNII lookup
VSW71SS07I	Internal UNII lookup
8E272251DI	Internal UNII lookup
6IO182RP7A	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
9aca850f-7e18-4147-aaf1-f6f04047f7f3	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139	Product name	3	20240506
e5a77e9c-c528-733a-173d-914a234c024b	Product name	5	20240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44911-0611-1	2023-11-17	C162847	48780-1	f386c64a-1d4a-0266-e053-dadaa90a7c1a	DRUG FACTS:
44911-0611-1	2023-01-30	C162847	48780-1	f386c64a-1d4a-0266-e053-dadaa90a7c1a	DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44911-0611-1	GI Clear P	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44911-0611	GI CLEAR P (ARSENICUM ALBUM, BAPTISIA TINCTORIA, LACHESIS MUTUS, PULSATILLA (PRATENSIS), RHUS TOX) LIQUID [ENERGIQUE, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250519_9aca850f-7e18-4147-aaf1-f6f04047f7f3.zip

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
GI Clear P	ARSENICUM ALBUM, BAPTISIA TINCTORIA, LACHESIS MUTUS, PULSATILLA (PRATENSIS), RHUS TOX	Energique, Inc.	9aca850f-7e18-4147-aaf1-f6f04047f7f3	2025-05-16	Warnings	Exact identifier ndc (package): 44911-0611-1 ndc (product): 44911-0611 ndc11 (package): 44911061101

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
S7V92P67HO	ARSENIC TRIOXIDE	1327-53-3	ARSENIC TRIOXIDE
5EF0HWI5WU	BAPTISIA TINCTORIA ROOT		BAPTISIA TINCTORIA ROOT
VSW71SS07I	LACHESIS MUTA VENOM		LACHESIS MUTA VENOM
6IO182RP7A	TOXICODENDRON PUBESCENS LEAF		TOXICODENDRON PUBESCENS LEAF

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
44911-0611-1	44911061101	60 mL in 1 BOTTLE, DROPPER (44911-0611-1)	60 ml	2021-06-21	2028-12-12	No	No	Current