FDA.reportPublic FDA data

Delay sprays for external-use

Manufacturer
Guangdong Hongfu Haohan Medical Instrument Co., Ltd.
Effective date
2021-11-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:15:11

Label at a glance#

ProductDelay sprays for external-use
Active ingredientEPIMEDIUM BREVICORNU WHOLE
Label structure11 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Epimedium Brevicornu Maxim 11% w/w

Purpose

OTC - PURPOSE SECTION

Delay function.

Reduce the sensitivity of the penis skin and improve the time of intercourse.

Warnings

WARNINGS SECTION

1.Those who are allergic to this product and minors are forbidden.
2.This product is a topical productand it is forbidden to take it orally.
3.Should not be used for the prevention of sexually transmitted diseases in sexual life.
4.Do not use on damaged mucosa wounds.
5.This productis a topical product and cannot be used as a substitute for drugs.
6.A small amount of precipitation during storage is normal and does not affect use.

When using

OTC - WHEN USING SECTION

By applying to the surface of the male penis skin, about 30 minutes before sex, spray an appropriate amount evenly on the glans and coronal sulcus.

Those who are allergic to this product and minors are forbidden.
This product is a topical productand it is forbidden to take it orally.
Should not be used for the prevention of sexually transmitted diseases in sexual life.
Do not use on damaged mucosa wounds.
This productis a topical product and cannot be used as a substitute for drugs.

A small amount of precipitation during storage is normal and does not affect use.

Do not use

OTC - DO NOT USE SECTION

Those who are allergic to this product and minors are forbidden.
This product is a topical productand it is forbidden to take it orally.
Should not be used for the prevention of sexually transmitted diseases in sexual life.
Do not use on damaged mucosa wounds.
This productis a topical product and cannot be used as a substitute for drugs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Scope of application

INDICATIONS & USAGE SECTION

By applying to the surface of the male penis skin,it can reduce the sensitivity of the penis skin and improve the time of intercourse.

USAGE METHOD

DOSAGE & ADMINISTRATION SECTION

About 30 minutes before sex, spray an appropriate amount evenly on the glans and coronal sulcus.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Zanthoxylum bungeanum, Syringa oblata Lindl, Lonicera Japonica, Cnidium monnieri (L.) Cuss, Carthamus tinctorius L, glycerol, Sodium methylparaben, phenoxyethanol, water.

Questions

OTC - QUESTIONS SECTION

After-sales service hotline: +86-0769-86864188

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bc0bb075-37ff-40b7-a924-cbc56a34f4dfProduct name220150616
15d6fc22-6acb-ed0a-b9b3-e5121820a5aaProduct name220150105
0695936f-2d11-d8f1-b51f-77f23a458cadProduct name120140508
1a8f0cfc-fa3a-e4fd-a79d-5f18408dcc9eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82408-301-012023-01-30C16284748780-1f386c649-a2dd-0266-e053-dadaa90a7c1aDelay sprays for external-use, 5mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82408-301-01Delay sprays for external-use5 g in 1 BOTTLELIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82408-301DELAY SPRAYS FOR EXTERNAL-USE (EPIMEDIUM BREVICORNU MAXIM) LIQUID [GUANGDONG HONGFU HAOHAN MEDICAL INSTRUMENT CO., LTD.]1Legacy NDC, 1 package rows20211123_d122b9b5-cde5-21d2-e053-2995a90a76da.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82408-30182408-301-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
CROCIN877GWI46C2IACT
GLYCERINPDC6A3C0OXIACT
METHYLPARABENA2I8C7HI9TIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
WATER059QF0KO0RIACT
OSTHOLXH1TI1759CIACT
METHOXSALENU4VJ29L7BQIACT
GARDENOSIDEINE79XNR2CIACT
EPIMEDIUM BREVICORNU WHOLE56UJF6417LACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d122b9b5-cde6-21d2-e053-2995a90a76dad122b9b5-cde5-21d2-e053-2995a90a76da2021-11-22WarningsExact identifier
spl id: d122b9b5-cde6-21d2-e053-2995a90a76da
spl set id: d122b9b5-cde5-21d2-e053-2995a90a76da

Reported adverse events (FAERS/openFDA)#

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