MEDICATED LIP BALM

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: MEDICATED LIP BALM
Generic name: MENTHOL AND EUCALYPTUS
Manufacturer: Burt's Bees, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 30da3cc5-6140-2dee-e054-00144ff8d46c
SPL ID: 7d8cda7b-4881-6d66-e053-2991aa0ab3ee
Version: 4
Effective date: 2018-12-21
Source export date: 2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:41:50

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		part348	openfda.application_number
brand name		MEDICATED LIP BALM	openfda.brand_name
generic name		MENTHOL AND EUCALYPTUS	openfda.generic_name
manufacturer name		Burt's Bees, Inc.	openfda.manufacturer_name
ndc	package	26052-029-02	openfda.package_ndc
ndc	package	26052-029-01	openfda.package_ndc
ndc	package	26052-029-03	openfda.package_ndc
ndc	package	26052-029-04	openfda.package_ndc
ndc	product	26052-029	openfda.product_ndc
ndc11	package	26052002903	derived:openfda.package_ndc
ndc11	package	26052002904	derived:openfda.package_ndc
ndc11	package	26052002901	derived:openfda.package_ndc
ndc11	package	26052002902	derived:openfda.package_ndc
spl id		7d8cda7b-4881-6d66-e053-2991aa0ab3ee	id
spl set id		30da3cc5-6140-2dee-e054-00144ff8d46c	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. IF CONDITION WORSENS OR IF SYMPTOMS PERSIST FOR MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS, DISCONTINUE USE AND CONSULT A DOCTOR. WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES KEEP OUT OF REACH OF CHUILDREN IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Reported adverse events (FAERS/openFDA)#

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