CHBO

Manufacturer
Xinshu Technology Co., Limited
Effective date
2026-02-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:45:57

Label at a glance#

ProductCHBO
Active ingredientVARDENAFIL, TADALAFIL
Label structure14 sections

Indications and uses

For the treatment of erectile dysfunction (ED)

Dosage and administration

Take one film by mouth, placed on the tongue to dissolve. Use 0.5 to 4 hours before sexual activity. Do not take more than once per day.

Label contents#

Full prescribing information#

Active ingredients (in each film)

OTC - ACTIVE INGREDIENT SECTION

Tadalafil 30 mg

Vardenafil 10 mg

Purpose

OTC - PURPOSE SECTION

Phosphodiesterase type 5 (PDE5) inhibitors

Uses

INDICATIONS & USAGE SECTION

For the treatment of erectile dysfunction (ED)

Warnings

WARNINGS SECTION

For adult men only.

Do not use if you:

OTC - DO NOT USE SECTION

take nitrate medicines (such as nitroglycerin)
have severe heart disease or very low blood pressure
are allergic to tadalafil, vardenafil, or any ingredient in this product
have galactose intolerance, total lactase deficiency, or glucose-galactose malabsorption

Ask a doctor before use if you have:

OTC - ASK DOCTOR SECTION

heart conditions, history of heart attack, irregular heartbeat, or chest pain
high or low blood pressure
liver or kidney disease
vision or hearing problems
history of priapism (painful or prolonged erection lasting >4 hours)
are over 65 years of age (higher risk of side effects, medical supervision advised)

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Take one film by mouth, placed on the tongue to dissolve.
Use 0.5 to 4 hours before sexual activity.
Do not take more than once per day.

When using this product you may experience:

OTC - WHEN USING SECTION

headache, flushing, indigestion, nasal congestion, dizziness, muscle pain, back pain, nausea, rash, or visual disturbances

Stop use and ask a doctor if:

OTC - STOP USE SECTION

you experience chest pain, fainting, sudden vision or hearing loss
an erection lasts longer than 4 hours (priapism). This is a medical emergency.

Drug Interactions

DRUG INTERACTIONS SECTION

Avoid use with: Nitrates, α-adrenergic blockers (e.g., tamsulosin), strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir, which may increase vardenafil plasma concentration).
Use with caution with: Antihypertensive drugs, alcohol (may enhance hypotensive effects).

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Contraindications

OTC - PREGNANCY OR BREAST FEEDING SECTION

Not for use in pregnant or breastfeeding women
Not for use in children under 18 years

Inactive ingredients

INACTIVE INGREDIENT SECTION

Film-forming polymers, stabilizers, sweeteners, flavoring agents.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2121

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
TADALAFIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
VARDENAFIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b90b74cb-f6c8-3798-d11c-73b8768b278aProduct name820250317
0fe0157c-95a7-4870-ae64-de9f3fa874aeProduct name120250227
20ae0006-d78c-4dba-9e3e-6ae424841903Product name120250127
b86a08b7-54cc-440b-ad4a-3e530ccd8324Product name620230421
7a02e74a-2844-42af-84a8-96bae57351cfProduct name120230313
928d249c-35c3-4d88-a9ef-cf2f2e31b96fProduct name120220706
f2f15561-f1f1-39f4-fff4-873c88c535cdProduct name420210224
9c8b57d3-6030-411c-8a17-97b4b8f0ea17Product name320200708

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87436-021-01CHBO1 in 1 POUCHFILM, SOLUBLE11
87436-021-01CHBO4 in 1 BOXFILM, SOLUBLE41

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87436-02187436-021-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
4ad86186-4acd-6204-e063-6394a90ac62e4ad86186-4acc-6204-e063-6394a90ac62e2026-02-15WarningsExact identifier
spl id: 4ad86186-4acd-6204-e063-6394a90ac62e
spl set id: 4ad86186-4acc-6204-e063-6394a90ac62e

Reported adverse events (FAERS/openFDA)#

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