Home FDA labels d44a9ea9-4e01-ec6c-e053-2a95a90a2bd5 EAR RX 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 EAR RX
Generic name ACONITUM NAP, BARYTA CARB, BELLADONNA, CALC CARB, CAPSICUM, CARBO VEG, CAUSTICUM, CHAMOMILLA, FERRUM PHOS, HEPAR SULPH CALC, KALI MUR, LACHESIS, LYCOPODIUM, MERCURIUS SOL, NATRUM MUR, PLANTAGO, PULSATILLA, SILICEA, SULPHUR, VERBASCUM
Manufacturer Miami Beach Pediatrics pa
Product type HUMAN OTC DRUG
SPL set ID a8753f88-4b8a-472f-a4bd-f2e9cec83610
SPL ID d44a9ea9-4e01-ec6c-e053-2a95a90a2bd5
Version 5
Effective date 2021-12-29
Source export date 2026-08-01
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/2026-08-01/4d7120b2932458966cd5c2f0e3ab49319f616f09498d059c9ff283a8dac64565/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run 20260801T225920Z
Imported at 2026-08-01 23:11:14 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 · 28 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name EAR RX openfda.brand_name generic name ACONITUM NAP, BARYTA CARB, BELLADONNA, CALC CARB, CAPSICUM, CARBO VEG, CAUSTICUM, CHAMOMILLA, FERRUM PHOS, HEPAR SULPH CALC, KALI MUR, LACHESIS, LYCOPODIUM, MERCURIUS SOL, NATRUM MUR, PLANTAGO, PULSATILLA, SILICEA, SULPHUR, VERBASCUM openfda.generic_name manufacturer name Miami Beach Pediatrics pa openfda.manufacturer_name ndc package 69390-001-01 openfda.package_ndc ndc product 69390-001 openfda.product_ndc ndc11 package 69390000101 derived:openfda.package_ndc spl id d44a9ea9-4e01-ec6c-e053-2a95a90a2bd5 id spl set id a8753f88-4b8a-472f-a4bd-f2e9cec83610 set_id unii 2P3VWU3H10 openfda.unii unii 00UK7646FG openfda.unii unii DD5FO1WKFU openfda.unii unii 324Y4038G2 openfda.unii unii C9TD27U172 openfda.unii unii 6P669D8HQ8 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 451W47IQ8X openfda.unii unii W2469WNO6U openfda.unii unii 2E32821G6I openfda.unii unii 91GQH8I5F7 openfda.unii unii 660YQ98I10 openfda.unii unii WQZ3G9PF0H openfda.unii unii 70FD1KFU70 openfda.unii unii VSW71SS07I openfda.unii unii U0NQ8555JD openfda.unii unii G0R4UBI2ZZ openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 openfda.unii unii 1MBW07J51Q 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: This product is to be used under the supervision of your healthcare provider. If symptoms worsen or persist for more than 5 days, consult your practitioner. IF PREGNANT OR NURSING, ask a health professional before use. KEEP OUT OF THE REACH OF CHILDREN.