Buzz Away Sting Soothe

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: Buzz Away Sting Soothe
Generic name: MENTHOL
Manufacturer: Quantum, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 419e34ea-17b2-ec32-e063-6394a90a603d
SPL ID: 419e34ea-17b3-ec32-e063-6394a90a603d
Version: 1
Effective date: 2025-10-20
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:17

Harmonized routes table
Harmonized routes
TOPICAL

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		M017	openfda.application_number
brand name		Buzz Away Sting Soothe	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Quantum, Inc.	openfda.manufacturer_name
ndc	package	70084-810-01	openfda.package_ndc
ndc	product	70084-810	openfda.product_ndc
ndc11	package	70084081001	derived:openfda.package_ndc
rxcui		1812747	openfda.rxcui
spl id		419e34ea-17b3-ec32-e063-6394a90a603d	id
spl set id		419e34ea-17b2-ec32-e063-6394a90a603d	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 For external use only When using this product, avoiid contact with eyes. Stop use and ask doctor if • condition worsens • symptoms last more than7 days or clear up and occuragain within a few days. If pregnant or nursing, ask a health professional. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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