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: 2026-10-27
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/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:07:28

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.