CARMEX Multi-Symptom 3 in 1 COLD Sore treatment External Analgesic Skin Protectant

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: CARMEX Multi-Symptom 3 in 1 COLD Sore treatment External Analgesic Skin Protectant
Generic name: BENZOCAINE, WHITE PETROLATUM
Manufacturer: Carma Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bbf0abcd-b7d6-b5e4-e053-2995a90a5240
SPL ID: 08883637-b8d6-23dc-e063-6394a90ae9f7
Version: 2
Effective date: 2023-10-25
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:02

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		CARMEX Multi-Symptom 3 in 1 COLD Sore treatment External Analgesic Skin Protectant	openfda.brand_name
generic name		BENZOCAINE, WHITE PETROLATUM	openfda.generic_name
manufacturer name		Carma Laboratories, Inc.	openfda.manufacturer_name
ndc	package	10210-0048-1	openfda.package_ndc
ndc	product	10210-0048	openfda.product_ndc
ndc11	package	10210004801	derived:openfda.package_ndc
rxcui		2479726	openfda.rxcui
spl id		08883637-b8d6-23dc-e063-6394a90ae9f7	id
spl set id		bbf0abcd-b7d6-b5e4-e053-2995a90a5240	set_id
unii		U3RSY48JW5	openfda.unii
unii		B6E5W8RQJ4	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 Allergy Alert: Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other “caine” anesthetic Stop use and ask a doctor or dentist if • cold sore symptoms do not improve in 7 days • irritation, pain, or redness persists or worsens • swelling, rash, or fever develops Do not use on • deep or puncture wounds • animal bites • serious burns When using this product keep out of eyes. Rinse with water to remove. Do not exceed recommended dosage. Keep out of reach of children. 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.