Hermon Balanitis relief kit

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: Hermon Balanitis relief kit
Generic name: SULFUR 1X HPUS
Manufacturer: Beautivity LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3dce086e-a4eb-4b21-e063-6394a90aa1b2
SPL ID: 3dce086e-a4ec-4b21-e063-6394a90aa1b2
Version: 1
Effective date: 2025-09-02
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 06:37:46

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Hermon Balanitis relief kit	openfda.brand_name
generic name		SULFUR 1X HPUS	openfda.generic_name
manufacturer name		Beautivity LLC	openfda.manufacturer_name
ndc	package	85398-013-01	openfda.package_ndc
ndc	package	85398-011-01	openfda.package_ndc
ndc	package	85398-014-01	openfda.package_ndc
ndc	product	85398-014	openfda.product_ndc
ndc11	package	85398001401	derived:openfda.package_ndc
ndc11	package	85398001301	derived:openfda.package_ndc
ndc11	package	85398001101	derived:openfda.package_ndc
rxcui		251267	openfda.rxcui
spl id		3dce086e-a4ec-4b21-e063-6394a90aa1b2	id
spl set id		3dce086e-a4eb-4b21-e063-6394a90aa1b2	set_id

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

For external use only children under 2 years of age unless directed by adoctor. avoid contact with the eyes. if contact occurs, rinse the eyes very thoroughly with water. if irritation occurs, symptoms persist for more than 2 weeks, or symptoms worsen after initial improvement lf 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.