NDC 69751-101-01 - Phexx

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 69751-101
Requested NDC: 69751-101-01
Package NDCs from labels: 69751-101-01, 69751-101-12
Manufacturer: Evofem, Inc.
Effective date: 2025-05-02
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Phexx - Evofem, Inc.	Evofem, Inc.	2025-05-02	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69751-101-01	Phexx	5 g in 1 APPLICATOR	GEL	5		2
69751-101-12	Phexx	12 in 1 BOX	GEL	12		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69751-101	PHEXX (LACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATE) GEL [EVOFEM, INC.]	2	Current NDC, 2 package rows	20250507_14b01a15-9b47-4be3-bb2e-a2010eab429e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69751-101-01	GM - Gram	69751-101	880012ce-db51-4b26-b064-9b8e753e1d27	1	2025-12-16
69751-101-12	GM - Gram	69751-101	eaad7137-d936-4224-bdb6-dd5aeecf1461	1	2025-11-13

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 8 of 8 · 143 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GUNA-ALLERGY-PREV	AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT -	Guna spa	adae93c0-1de9-4e45-ab58-148171f0dc86	2018-12-21	Warnings	Exact identifier unii: 2968PHW8QP
Metabolism Manager	ASCLEPIAS VINCETOXICUM, ECHINACEA (ANGUSTIFOLIA), HYPOTHALAMUS SUIS, CEREBRUM SUIS, HEPAR SUIS, KIDNEY (SUIS), METHYLCOBALAMIN, PANCREAS SUIS, STOMACH (SUIS), AACG-A, AACG-B, CALCAREA CARBONICA, GAMBOGIA, GELSEMIUM SEMPERVIRENS, GRAPHITES, NUX VOMICA, PHYTOLACCA DECANDRA, 7-OXO-DEHYDROEPIANDROSTERONE-3BETA-ACETATE (7-KETO), ADENOSINUM TRIPHOSPHORICUM DINATRUM, GLUCAGON, INSULINUM (SUIS), SARCOLACTICUM ACIDUM, PROTEUS (VULGARIS)	Healthsource of New England LLC	3ea3bc94-6c36-49a2-8cdf-70b3ad45accb	2018-08-22	Warnings	Exact identifier unii: F9S9FFU82N
Weight Management Support	ASCLEPIAS VINCETOXICUM, ECHINACEA (ANGUSTIFOLIA), HYPOTHALAMUS (SUIS), CEREBRUM (SUIS), HEPAR SUIS, KIDNEY (SUIS), METHYLCOBALAMIN, PANCREAS SUIS, STOMACH (SUIS), AACG-A, AACG-B, CALCAREA CARBONICA, GAMBOGIA, GELSEMIUM SEMPERVIRENS, GRAPHITES, NUX VOMICA, PHYTOLACCA DECANDRA, 7-KETO (3-ACETYL-7-OXO-DEHYDROEPIANDROSTERONE), ADENOSINUM TRIPHOSPHORICUM DINATRUM, GLUCAGON, INSULINUM, SARCOLACTICUM ACIDUM, PROTEUS (VULGARIS)	Lifetime Fat Loss Centers	940ca77c-2f80-4457-a31d-08dc70e89805	2016-06-23	Warnings	Exact identifier unii: F9S9FFU82N

Reported adverse events (FAERS/openFDA)#

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