Home FDA labels b3523678-6826-433e-8ee3-a0a57c07037a Cold 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
Generic name BAPTISIA TINCTORIA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM, LOMATIUM DISSECTUM, PUERARIA LOBATA, TRIFOLIUM PRATENSE, PHYTOLACCA DECANDRA, ALLIUM CEPA, ARSENICUM IODATUM, BARYTA CARBONICA, BROMIUM, CALCAREA CARBONICA, KALI MURIATICUM, LACHESIS MUTUS, MERCURIUS SOLUBILIS, SILICEA
Manufacturer Natural Creations, Inc
Product type HUMAN OTC DRUG
SPL set ID c45d1d8f-24be-4c13-8c4b-388962421415
SPL ID b3523678-6826-433e-8ee3-a0a57c07037a
Version 2
Effective date 2025-11-20
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 01:47:11 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 Cold openfda.brand_name generic name BAPTISIA TINCTORIA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM, LOMATIUM DISSECTUM, PUERARIA LOBATA, TRIFOLIUM PRATENSE, PHYTOLACCA DECANDRA, ALLIUM CEPA, ARSENICUM IODATUM, BARYTA CARBONICA, BROMIUM, CALCAREA CARBONICA, KALI MURIATICUM, LACHESIS MUTUS, MERCURIUS SOLUBILIS, SILICEA openfda.generic_name manufacturer name Natural Creations, Inc openfda.manufacturer_name ndc package 43406-0688-1 openfda.package_ndc ndc product 43406-0688 openfda.product_ndc ndc11 package 43406068801 derived:openfda.package_ndc spl id b3523678-6826-433e-8ee3-a0a57c07037a id spl set id c45d1d8f-24be-4c13-8c4b-388962421415 set_id unii 11E6VI8VEG openfda.unii unii SBV4XY874G openfda.unii unii D295OFK7E1 openfda.unii unii 324Y4038G2 openfda.unii unii 5K1UO2888Y openfda.unii unii 3029988O2T openfda.unii unii 6P669D8HQ8 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 2E32821G6I openfda.unii unii VB06AV5US8 openfda.unii unii 660YQ98I10 openfda.unii unii 492225Q21H openfda.unii unii 5329928G5N openfda.unii unii VSW71SS07I openfda.unii unii 1W0775VX6E openfda.unii unii 4JS0838828 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: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. A persistent cough may be a sign of a serious condition. If cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache, consult a doctor. Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.