Manuka Honey Extra Strength

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: Manuka Honey Extra Strength
Generic name: ALLANTOIN
Manufacturer: First Honey LLC
Product type: HUMAN OTC DRUG
SPL set ID: b742585d-9a0c-489b-b268-590583cfabd1
SPL ID: 2d5e1f54-b018-fce5-e063-6394a90a76d7
Version: 3
Effective date: 2025-02-04
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:03

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Manuka Honey Extra Strength	openfda.brand_name
generic name		ALLANTOIN	openfda.generic_name
manufacturer name		First Honey LLC	openfda.manufacturer_name
ndc	package	81995-050-01	openfda.package_ndc
ndc	product	81995-050	openfda.product_ndc
ndc11	package	81995005001	derived:openfda.package_ndc
spl id		2d5e1f54-b018-fce5-e063-6394a90a76d7	id
spl set id		b742585d-9a0c-489b-b268-590583cfabd1	set_id
unii		344S277G0Z	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 Do not use In the eyes On deep or puncture wounds Animal bites Serious burns Stop use and ask a doctor if Conditions worsen Symptoms last more than 7 days or clear up and occur again within a few days 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.