Home FDA labels 6a28ccf7-80a2-4db1-a1aa-ec417335b8ae Fem Flora Defense openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Fem Flora Defense
Generic name BAPTISIA TINCTORIA, BORAX, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, CINCHONA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), NITRICUM ACIDUM, PULSATILLA (PRATENSIS), PYROGENIUM, SEPIA, SULPHURICUM ACIDUM, THUJA OCCIDENTALIS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 8015e1cb-9ebd-4b3e-af57-92f2754fb790
SPL ID 6a28ccf7-80a2-4db1-a1aa-ec417335b8ae
Version 2
Effective date 2023-08-17
Source export date 2026-09-28
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:08 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Fem Flora Defense openfda.brand_name generic name BAPTISIA TINCTORIA, BORAX, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, CINCHONA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), NITRICUM ACIDUM, PULSATILLA (PRATENSIS), PYROGENIUM, SEPIA, SULPHURICUM ACIDUM, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0274-1 openfda.package_ndc ndc product 50845-0274 openfda.product_ndc ndc11 package 50845027401 derived:openfda.package_ndc spl id 6a28ccf7-80a2-4db1-a1aa-ec417335b8ae id spl set id 8015e1cb-9ebd-4b3e-af57-92f2754fb790 set_id unii 411VRN1TV4 openfda.unii unii 91MBZ8H3QO openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii 29SUH5R3HU openfda.unii unii 4D7G21HDBC openfda.unii unii VB06AV5US8 openfda.unii unii O40UQP6WCF openfda.unii unii 8E272251DI openfda.unii unii S003A158SB openfda.unii unii 0KZ676D44N openfda.unii unii 5EF0HWI5WU openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If symptoms persist for more than 7 days, consult a doctor. If pregnant or breast feeding, ask a doctor before use. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.