FDA.reportPublic FDA data

Uterus 13X

Product NDC
53645-2540
Requested package NDC
53645-2540-6
11-digit product format
536452540
Labeler code
53645
Product ID
53645-2540_522dc678-ab93-e381-e063-6394a90abedc
Type
HUMAN OTC DRUG
Nonproprietary name
Uterus 13X
Dosage form
LIQUID
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-05-19
Substance
BOS TAURUS UTERUS
Active strength
13 [hp_X]/30mL
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Uterus 13X
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BOS TAURUS UTERUS13 [hp_X]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9169LW451GInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
522de56a-7aaa-0ba3-e063-6394a90ad458Available on FDA.report

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
Uterus 13XUTERUS 13XTrue Botanica, LLC522de56a-7aaa-0ba3-e063-6394a90ad4582026-05-19WarningsExact identifier
ndc (package): 53645-2540-6
ndc (product): 53645-2540
ndc11 (package): 53645254006

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleStatus
53645-2540-65364525400630 mL in 1 BOTTLE (53645-2540-6)30 ml2026-05-190Current