Home FDA labels 295ea3ec-7e83-4c0f-bef6-3083376f5913 Apnetem 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 Apnetem
Generic name PHOSPHORICUM ACIDUM, ALUMEN, PHOSPHORUS, SENEGA OFFICINALIS, ADENOSINUM CYCLOPHOSPHORICUM, ANTIMONIUM TARTARICUM, GRINDELIA, SABADILLA, ALUMINA, CUPRUM METALLICUM, SANGUINARINUM NITRICUM, SILICEA, LACHESIS MUTUS, RHEUM (PALMATUM), ZINCUM METALLICUM, LYCOPODIUM CLAVATUM, MANGANUM PHOSPHORICUM, ANTIPYRINUM, COENZYME A
Manufacturer Nucleic Products, LLC
Product type HUMAN OTC DRUG
SPL set ID ec5bc7e7-4be6-45a6-8cd9-62fdfa7fb469
SPL ID 295ea3ec-7e83-4c0f-bef6-3083376f5913
Version 13
Effective date 2025-05-14
Source export date 2026-10-27
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 19:45:34 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 Apnetem openfda.brand_name generic name PHOSPHORICUM ACIDUM, ALUMEN, PHOSPHORUS, SENEGA OFFICINALIS, ADENOSINUM CYCLOPHOSPHORICUM, ANTIMONIUM TARTARICUM, GRINDELIA, SABADILLA, ALUMINA, CUPRUM METALLICUM, SANGUINARINUM NITRICUM, SILICEA, LACHESIS MUTUS, RHEUM (PALMATUM), ZINCUM METALLICUM, LYCOPODIUM CLAVATUM, MANGANUM PHOSPHORICUM, ANTIPYRINUM, COENZYME A openfda.generic_name manufacturer name Nucleic Products, LLC openfda.manufacturer_name ndc package 75053-0008-1 openfda.package_ndc ndc product 75053-0008 openfda.product_ndc ndc11 package 75053000801 derived:openfda.package_ndc spl id 295ea3ec-7e83-4c0f-bef6-3083376f5913 id spl set id ec5bc7e7-4be6-45a6-8cd9-62fdfa7fb469 set_id unii 27YLU75U4W openfda.unii unii LMI26O6933 openfda.unii unii 789U1901C5 openfda.unii unii VZ3U1H7Q5B openfda.unii unii T3CHA1B51H openfda.unii unii SAA04E81UX openfda.unii unii DL6OZ476V3 openfda.unii unii G025DAL7CE openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 1L24V9R23S openfda.unii unii 6NAF1689IO openfda.unii unii E0399OZS9N openfda.unii unii M7T6H7D4IF openfda.unii unii BOP122S791 openfda.unii unii VSW71SS07I openfda.unii unii E4GA8884NN openfda.unii unii IDB0NAZ6AI openfda.unii unii J41CSQ7QDS openfda.unii unii C88X29Y479 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: As with any drug, ask a doctor before use if pregnant or nursing. Warning - Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physicians promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by physician. Keep this and all medications out of the reach of children. In case of accidental overdose, contact a medical professional or poison control center immediately.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.