FDA.reportPublic FDA data

Menopause Relief

Product NDC
57955-9973
11-digit product format
579559973
Labeler code
57955
Product ID
57955-9973_6fdc80e5-9b13-4bc0-b1da-305fdcb98463
Type
HUMAN OTC DRUG
Nonproprietary name
Amyl nit, Calc carb, Caulophyllum, Cimicifuga, Ferrum met, Gelsemium, Lachesis, Pulsatilla, Sanguinaria, Sepia, Sulphur and Sulphuricum ac.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-03-13
Substance
AMYL NITRITE; BLACK COHOSH; CAULOPHYLLUM THALICTROIDES ROOT; GELSEMIUM SEMPERVIRENS ROOT; IRON; LACHESIS MUTA VENOM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PULSATILLA VULGARIS WHOLE; SANGUINARIA CANADENSIS ROOT; SEPIA OFFICINALIS JUICE; SULFUR; SULFURIC ACID
Active strength
10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Menopause Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMYL NITRITE10 [hp_X]/59mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE10 [hp_X]/59mL
CAULOPHYLLUM THALICTROIDES ROOT10 [hp_X]/59mL
BLACK COHOSH10 [hp_X]/59mL
IRON10 [hp_X]/59mL
GELSEMIUM SEMPERVIRENS ROOT10 [hp_X]/59mL
LACHESIS MUTA VENOM10 [hp_X]/59mL
PULSATILLA VULGARIS WHOLE10 [hp_X]/59mL
SANGUINARIA CANADENSIS ROOT10 [hp_X]/59mL
SEPIA OFFICINALIS JUICE10 [hp_X]/59mL
SULFUR10 [hp_X]/59mL
SULFURIC ACID10 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 12 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
22T8Z09XAKInternal UNII lookup
2E32821G6IInternal UNII lookup
JTJ6HH6YEHInternal UNII lookup
K73E24S6X9Internal UNII lookup
E1UOL152H7Internal UNII lookup
639KR60Q1QInternal UNII lookup
VSW71SS07IInternal UNII lookup
I76KB35JEVInternal UNII lookup
N9288CD508Internal UNII lookup
QDL83WN8C2Internal UNII lookup
70FD1KFU70Internal UNII lookup
O40UQP6WCFInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
e12b75f5-6c5f-4b39-a6aa-dad07089f1d8Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-9973-2Menopause Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Menopause ReliefAMYL NIT, CALC CARB, CAULOPHYLLUM, CIMICIFUGA, FERRUM MET, GELSEMIUM, LACHESIS, PULSATILLA, SANGUINARIA, SEPIA, SULPHUR AND SULPHURICUM AC.King Bio Inc.e12b75f5-6c5f-4b39-a6aa-dad07089f1d82026-03-10WarningsExact identifier
ndc (product): 57955-9973

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
57955-9973-25795599730259 mL in 1 BOTTLE, SPRAY (57955-9973-2) 59 ml2026-03-13NoNoCurrent