WALGREENS EARACHE DROPS

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: WALGREENS EARACHE DROPS
Generic name: BELLADONNA LEAF, CALCIUM CARBONATE, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, ANEMONE PATENS, AND SULFUR
Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
SPL set ID: c573dc3c-992e-604d-e053-2995a90a0ff4
SPL ID: 43f4e055-220f-beba-e063-6394a90a1085
Version: 3
Effective date: 2025-11-19
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:44

Harmonized routes table
Harmonized routes
AURICULAR (OTIC)

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		WALGREENS EARACHE DROPS	openfda.brand_name
generic name		BELLADONNA LEAF, CALCIUM CARBONATE, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, ANEMONE PATENS, AND SULFUR	openfda.generic_name
manufacturer name		Walgreen Company	openfda.manufacturer_name
ndc	package	0363-3233-15	openfda.package_ndc
ndc	product	0363-3233	openfda.product_ndc
ndc11	package	00363323315	derived:openfda.package_ndc
spl id		43f4e055-220f-beba-e063-6394a90a1085	id
spl set id		c573dc3c-992e-604d-e053-2995a90a0ff4	set_id
unii		4M1169RWJD	openfda.unii
unii		H0G9379FGK	openfda.unii
unii		FGL3685T2X	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		6GZW20TIOI	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 USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN AND UNDER THE SUPERVISION OF A PHYSICIAN. • Keep away from eyes. • Do not take by mouth. • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur. • A Physician should always be consulted to rule out serious causes. • If accidental contact with eyes occurs, flush eyes with water and consult a doctor. • If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children. • If swallowed, get medical help or contact a Poison Control Center right away. Do not use: • If you have ear drainage, irritation, discharge or rash in the ear, consult a physician • With ear tubes, damaged ear drums or after surgery. • If drops become cloudy.

Reported adverse events (FAERS/openFDA)#

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