Home FDA labels 473bff35-5772-4fe3-a79f-318eeae9024b Hers Plus 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 Hers Plus
Generic name CALENDULA OFFICINALIS, SAMBUCUS NIGRA, ALLIUM SATIVUM, CLEMATIS ERECTA, DULCAMARA, SARSAPARILLA (SMILAX REGELII), GRAPHITES, PETROLEUM, ARSENICUM ALBUM, CROTON TIGLIUM, MERCURIUS SULPHURATUS RUBER, NATRUM MURIATICUM, NITRICUM ACIDUM, RHUS TOX, SEPIA, THUJA OCCIDENTALIS
Manufacturer Deseret Biologicals,Inc.
Product type HUMAN OTC DRUG
SPL set ID e4636b80-f6c8-459c-8d0e-ff7801358b10
SPL ID 473bff35-5772-4fe3-a79f-318eeae9024b
Version 4
Effective date 2024-04-09
Source export date 2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:47:10 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Hers Plus openfda.brand_name generic name CALENDULA OFFICINALIS, SAMBUCUS NIGRA, ALLIUM SATIVUM, CLEMATIS ERECTA, DULCAMARA, SARSAPARILLA (SMILAX REGELII), GRAPHITES, PETROLEUM, ARSENICUM ALBUM, CROTON TIGLIUM, MERCURIUS SULPHURATUS RUBER, NATRUM MURIATICUM, NITRICUM ACIDUM, RHUS TOX, SEPIA, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Deseret Biologicals,Inc. openfda.manufacturer_name ndc package 43742-1876-1 openfda.package_ndc ndc product 43742-1876 openfda.product_ndc ndc11 package 43742187601 derived:openfda.package_ndc spl id 473bff35-5772-4fe3-a79f-318eeae9024b id spl set id e4636b80-f6c8-459c-8d0e-ff7801358b10 set_id unii V1V998DC17 openfda.unii unii KPS1B1162N openfda.unii unii 2H1576D5WG openfda.unii unii 4QQN74LH4O openfda.unii unii 411VRN1TV4 openfda.unii unii 18E7415PXQ openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii 451W47IQ8X openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii 0HK2GZK66E openfda.unii unii CT03BSA18U openfda.unii unii ZI0T668SF1 openfda.unii unii 1C89KKC04E openfda.unii unii 396421SP9F 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 WARNING: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.