Progesterone

Product NDC: 43857-0103
11-digit product format: 438570103
Labeler code: 43857
Product ID: 43857-0103_d1c58e66-a542-42a8-b67a-8928a8c07c2d
Type: HUMAN OTC DRUG
Nonproprietary name: Progesterone
Dosage form: LIQUID
Route: ORAL
Labeler: BioActive Nutritional, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2013-02-12
Substance: PROGESTERONE
Active strength: 6 [hp_X]/mL
Pharmacologic classes: Progesterone [CS], Progesterone [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Progesterone
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PROGESTERONE	6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4G7DS2Q64Y	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
0de91238-dacc-4a5c-86d8-ad94024b2c95	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b46148e2-ee15-98d5-12f0-f5ec8745f6fc	Product name	3	20220927
76820076-f087-4073-b1d1-aa04b361335e	Product name	2	20220921
d3229c1a-4e51-4e04-9b13-00d24fd35242	Product name	1	20200821
213f0591-95c1-b398-40b7-08b31f66b026	Product name	4	20190206
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810
85b2d644-53b2-f2dc-4dbc-859116ce56c0	Product name	1	20140508
d048f0e3-3c40-8816-8c5c-0ca5cd189aac	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43857-0103-1	Progesterone	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PROGESTERONE	ACTIVE INGREDIENT	4G7DS2Q64Y	PROGESTERONE LIQUID [BIOACTIVE NUTRITIONAL, INC.]	1
PROGESTERONE	ACTIVE MOIETY	4G7DS2Q64Y	PROGESTERONE LIQUID [BIOACTIVE NUTRITIONAL, INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	PROGESTERONE LIQUID [BIOACTIVE NUTRITIONAL, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	PROGESTERONE LIQUID [BIOACTIVE NUTRITIONAL, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43857-0103	PROGESTERONE LIQUID [BIOACTIVE NUTRITIONAL, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250522_0de91238-dacc-4a5c-86d8-ad94024b2c95.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
Progesterone	PROGESTERONE	BioActive Nutritional, Inc.	0de91238-dacc-4a5c-86d8-ad94024b2c95	2025-05-20	Warnings	Exact identifier ndc (product): 43857-0103

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4G7DS2Q64Y	PROGESTERONE	57-83-0	PROGESTERONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
43857-0103-1	43857010301	30 mL in 1 BOTTLE, DROPPER (43857-0103-1)	30 ml	2016-04-14	0000-00-00	No	No	Current