Menopause Plus Moisture

Product NDC: 54973-3358
11-digit product format: 549733358
Labeler code: 54973
Product ID: 54973-3358_efa78986-38f2-f817-e053-2995a90a2ad7
Type: HUMAN OTC DRUG
Nonproprietary name: ATROPA BELLADONNA, BERBERIS VULGARIS ROOT BARK, CAULOPHYLLUM THALICTROIDES ROOT, BLACK COHOSH, GRAPHITE, LACHESIS MUTA VENOM, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, DELPHINIUM STAPHISAGRIA SEED and SULFUR
Dosage form: KIT
Route: SUBLINGUAL
Labeler: Hyland's Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2018-06-01
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	54973-3358		D	Discontinued by firm		2026-10-05
excluded package	package	54973-3358	54973-3358-1	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	54973-3358-1	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	54973-3358-1	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
54973-3358-1	2022-10-20	C162847	48780-1	e4f33bdf-ac85-d8a0-e053-dadaa90a6e4e	Doctor Wise Menopause+ Moisture
54973-3358-1	2022-07-29	C162847	48780-1	e4f33bdf-ac85-d8a0-e053-dadaa90a6e4e	Doctor Wise Menopause+ Moisture

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54973-3358	MENOPAUSE PLUS MOISTURE (ATROPA BELLADONNA, BERBERIS VULGARIS ROOT BARK, CAULOPHYLLUM THALICTROIDES ROOT, BLACK COHOSH, GRAPHITE, LACHESIS MUTA VENOM, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, DELPHINIUM STAPHISAGRIA SEED AND SULFUR) KIT [HYLAND'S INC.]	2	Legacy NDC	20221213_6b15fbeb-528b-050c-e053-2991aa0a4eca.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
54973-3358-1	54973335801	1 KIT in 1 CARTON (54973-3358-1) * 60 TABLET in 1 BOTTLE, PLASTIC (54973-3357-1) * 4 TABLET in 1 PACKET (54973-3357-2)	1 kit	2018-06-01	0000-00-00	No	No	Current