Home FDA labels b985df4b-c2ff-40bf-9d3f-a425781d3354 Cold Sore Formula 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 Cold Sore Formula
Generic name DULCAMARA, GLYCYRRHIZA GLABRA, RANUNCULUS BULBOSUS, RHUS TOX, NATRUM MURIATICUM, FAGOPYRUM ESCULENTUM, NATRUM HYPOCHLOROUS, ACONITUM NAPELLUS, CYTOMEGALOVIRUS NOSODE, HERPES SIMPLEX I AND II NOSODE, SEPIA, EPSTEIN BARR VIRUS NOSODE, HERPES ZOSTER NOSODE, ADENOVIREN NOSODE
Manufacturer Nutritional Specialties, Inc.
Product type HUMAN OTC DRUG
SPL set ID ad6a08ec-5eba-405b-8a07-79ac86ab3e7a
SPL ID b985df4b-c2ff-40bf-9d3f-a425781d3354
Version 1
Effective date 2026-03-31
Source export date 2026-10-27
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:50:16 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Cold Sore Formula openfda.brand_name generic name DULCAMARA, GLYCYRRHIZA GLABRA, RANUNCULUS BULBOSUS, RHUS TOX, NATRUM MURIATICUM, FAGOPYRUM ESCULENTUM, NATRUM HYPOCHLOROUS, ACONITUM NAPELLUS, CYTOMEGALOVIRUS NOSODE, HERPES SIMPLEX I AND II NOSODE, SEPIA, EPSTEIN BARR VIRUS NOSODE, HERPES ZOSTER NOSODE, ADENOVIREN NOSODE openfda.generic_name manufacturer name Nutritional Specialties, Inc. openfda.manufacturer_name ndc package 83027-0303-1 openfda.package_ndc ndc product 83027-0303 openfda.product_ndc ndc11 package 83027030301 derived:openfda.package_ndc spl id b985df4b-c2ff-40bf-9d3f-a425781d3354 id spl set id ad6a08ec-5eba-405b-8a07-79ac86ab3e7a set_id unii 2788Z9758H openfda.unii unii 74J6DNH49U openfda.unii unii 22G38P19RL openfda.unii unii KPS1B1162N openfda.unii unii 9885M7D6JP openfda.unii unii QDL83WN8C2 openfda.unii unii 2A26YW7PNX openfda.unii unii DY38VHM5OD openfda.unii unii FKD3DUK39I openfda.unii unii 451W47IQ8X openfda.unii unii 6IO182RP7A openfda.unii unii AEQ8NXJ0MB openfda.unii unii B10M69172N openfda.unii unii U0NQ8555JD openfda.unii unii 7COI029E6K 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 breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.