Home FDA labels 10a1e1cb-fffe-4e2f-885d-0350ec19965e Intimate 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 Intimate
Generic name ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA (HUMAN), GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 066bd402-378b-48aa-9515-188c261a3f4c
SPL ID 10a1e1cb-fffe-4e2f-885d-0350ec19965e
Version 2
Effective date 2025-05-27
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:21 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 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Intimate openfda.brand_name generic name ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA (HUMAN), GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2185-1 openfda.package_ndc ndc product 43742-2185 openfda.product_ndc ndc11 package 43742218501 derived:openfda.package_ndc spl id 10a1e1cb-fffe-4e2f-885d-0350ec19965e id spl set id 066bd402-378b-48aa-9515-188c261a3f4c set_id unii C151H8M554 openfda.unii unii 51FI676N6F openfda.unii unii 7YNJ3PO35Z openfda.unii unii C8CV8867O8 openfda.unii unii 608DGJ6815 openfda.unii unii 1NT28V9397 openfda.unii unii G39P120JQT openfda.unii unii 1JQS135EYN openfda.unii unii 4VB4Y46AHD openfda.unii unii N20HL7Q941 openfda.unii unii RHH784E0K6 openfda.unii unii 3A3U0GI71G openfda.unii unii G6W4F0V8Z3 openfda.unii unii 45P3261C7T openfda.unii unii Y0F0BU8RDU openfda.unii unii 00072J7XWS openfda.unii unii 2BMD2GNA4V openfda.unii unii 7FT6QUT299 openfda.unii unii 1XCH439UQR 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 pregnant or breastfeeding, 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.