Strawberry Cough 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: Strawberry Cough Drops
Generic name: MENTHOL
Manufacturer: BestCo Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 26a22cfd-395b-4ffb-e054-00144ff88e88
SPL ID: 47467544-a0d3-1d4e-e063-6394a90a1bb3
Version: 8
Effective date: 2025-12-31
Source export date: 2026-11-06
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/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:50:46

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Strawberry Cough Drops	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		BestCo Inc.	openfda.manufacturer_name
ndc	package	52642-020-30	openfda.package_ndc
ndc	product	52642-020	openfda.product_ndc
ndc11	package	52642002030	derived:openfda.package_ndc
rxcui		433196	openfda.rxcui
spl id		47467544-a0d3-1d4e-e063-6394a90a1bb3	id
spl set id		26a22cfd-395b-4ffb-e054-00144ff88e88	set_id
unii		L7T10EIP3A	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 Sore Throat Warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

Reported adverse events (FAERS/openFDA)#

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