Lidocaine PS Cream 73581-022

Manufacturer
YYBA Corp
Effective date
2026-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:58:49

Label at a glance#

ProductLidocaine
Active ingredientLIDOCAINE
Label structure11 sections

Indications and uses

■ Helps relieve the local itching and discomfort in the perianal area ■ For the temporary relief of pain, irritation or burning ■ Temporarily shrinks hemorrhoidal tissue.

Dosage and administration

Adults: ■ When practical, cleanse the affected area with mild soap and warm water and rinse by patting or blotting with an appropriate cleansing pad ■ Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. ■ Children under 12 years of age: consult a doctor. ■ Apply externally to the affected area up to 6 times daily or after each bowel movement.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Anorectal (hemorrhoidal) cream

Uses

INDICATIONS & USAGE SECTION

■ Helps relieve the local itching and discomfort in the perianal area
■ For the temporary relief of pain, irritation or burning
■ Temporarily shrinks hemorrhoidal tissue.

Warnings

WARNINGS SECTION

____________________________________________________________

For external use only

WARNINGS SECTION

Do not ■ exceed the recommended daily dosage unless directed by a
doctor ■ put this product into the rectum by using your fingers or any
mechanical device or applicator. ■ use this product if you have heart
disease, high blood pressure, thyroid disease, diabetes, or difficulty
in urination due to enlargement of the prostate gland unless directed
by a doctor

When using this product

OTC - WHEN USING SECTION

■ if the condition worsens or does not improve,
within 7 days consult a doctor ■in case of bleeding consult a doctor promptly.

Stop use

OTC - STOP USE SECTION

■ If the symptoms being treated do not subside or if redness,
irritation, swelling, pain, or other symptoms develop or increase.

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

■ presently taking a prescription drug for high blood pressure or depression.

Allergy alert

OTHER SAFETY INFORMATION

■ Certain persons can develop allergic reactions to ingredients in this product. taking a prescription drug for high blood
pressure or depression.

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 right away. If pregnant or breast-feeding,
ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: ■ When practical, cleanse the affected area with mild
soap and warm water and rinse by patting or blotting with an appropriate
cleansing pad ■ Gently dry by patting or blotting with toilet tissue or
a soft cloth before application of this product. ■ Children under 12
years of age: consult a doctor. ■ Apply externally to the affected area
up to 6 times daily or after each bowel movement.

Other information

SPL UNCLASSIFIED SECTION

■ Protect the product in this container from excessive
heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Cetearyl Alcohol, Disodium EDTA,
Ethylhexylglycerin, Glyceryl Stearate, Glycine Soja (Soybean) Oil, Isopropyl
Myristate, PEG-100 Stearate, Phenoxyethanol, Propylene Glycol, Stearic Acid,
Tocopherol, Triethanolamine, Water (Aqua)

Questions?

OTC - QUESTIONS SECTION

call 1-866-933-6337

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1534792lidocaine 5 % Topical CreamPSN1
1534792lidocaine 50 MG/ML Topical CreamSCD1
1534792lidocaine 5 % Topical CreamSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73581-022-06Lidocaine170 mL in 1 JARCREAM1701

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73581-02273581-022-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
LidocaineLIDOCAINEYYBA Corp5256a84a-8dac-8fd4-e063-6294a90a616c2026-04-01WarningsExact identifier
ndc (package): 73581-022-06
ndc (product): 73581-022
ndc11 (package): 73581002206
spl id: 5256a84a-8dad-8fd4-e063-6294a90a616c
spl set id: 5256a84a-8dac-8fd4-e063-6294a90a616c

Reported adverse events (FAERS/openFDA)#

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