Lidophen QCDMO

Manufacturer
YYBA CORP
Effective date
2026-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-05 01:01:14

Label at a glance#

ProductLidocaine Phenylephrine
Active ingredientLIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE
Label structure13 sections

Dosage and administration

when practical, cleanse the affected area with mild soap and warm water rinse thoroughly and gently pat dry spray affected area wash hands after applying replace cap after use Adults and children 12 years or older: apply externally to affected area not more than 4 times daily Children under 12 years of age: do not use, ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

Phenylephrine HCl .25%

Purpose

OTC - PURPOSE SECTION

Local anesthetic

Vasoconstrictor

Use

INDICATIONS & USAGE SECTION

temporarily reduces swelling associated with irritated hemorrhoidal tissue and other anorectal disorders

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes
  • do not exceed recommended dosage unless directed by a doctor
  • do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rectal bleeding occurs
  • treated symptom does not subside or redness, irritation, swelling, pain, or other symptoms develop or increase

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • when practical, cleanse the affected area with mild soap and warm water
  • rinse thoroughly and gently pat dry
  • spray affected area
  • wash hands after applying
  • replace cap after use

Adults and children 12 years or older:

  • apply externally to affected area not more than 4 times daily

Children under 12 years of age:

  • do not use, ask a doctor

Other information

SPL UNCLASSIFIED SECTION

Store out of direct sunlight, in a cool dry, well-ventilated area. Do not store at temperature above 120 degrees farenheit (49 degrees celsius)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citric Acid, Disodium EDTA, DL-Panthenol, Glycerin, Isopropyl Myristate, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Purified Water.

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-866-933-6337

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130373581001194GTIN-13: 0373581001194
EAN-13: 0373581001194
GTIN-12: 373581001194
UPC-A: 373581001194
GTIN storage (14 digits): 00373581001194
lidophenlabel.jpg

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73581-91073581-910-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Lidocaine PhenylephrineLIDOCAINE PHENYLEPHRINEYYBA CORP5a72a190-2129-411e-e063-6394a90a08c22026-09-01WarningsExact identifier
ndc (package): 73581-910-01
ndc (product): 73581-910
ndc11 (package): 73581091001
spl id: 5a72a190-212a-411e-e063-6394a90a08c2
spl set id: 5a72a190-2129-411e-e063-6394a90a08c2

Reported adverse events (FAERS/openFDA)#

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