Cold Sore Fever Blister Treatment

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: Cold Sore Fever Blister Treatment
Generic name: DOCOSANOL
Manufacturer: H E B
Product type: HUMAN OTC DRUG
SPL set ID: 98726ef3-ae48-4447-86de-17d37d2324cd
SPL ID: 9ecb26a2-7d32-482b-8c7c-3051be0d63d6
Version: 5
Effective date: 2023-07-19
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:02

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 applno	ANDA	212385	derived:openfda.application_number
application number		ANDA212385	openfda.application_number
brand name		Cold Sore Fever Blister Treatment	openfda.brand_name
generic name		DOCOSANOL	openfda.generic_name
manufacturer name		H E B	openfda.manufacturer_name
ndc	package	37808-765-07	openfda.package_ndc
ndc	product	37808-765	openfda.product_ndc
ndc11	package	37808076507	derived:openfda.package_ndc
rxcui		797534	openfda.rxcui
spl id		9ecb26a2-7d32-482b-8c7c-3051be0d63d6	id
spl set id		98726ef3-ae48-4447-86de-17d37d2324cd	set_id
unii		9G1OE216XY	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 Allergy Alert: This product may cause a severe allergic reaction. Symptoms may include: hives facial swelling wheezing/difficulty shock rash If an allergic reaction occurs, stop use and seek medical help right away. For external use only

Reported adverse events (FAERS/openFDA)#

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