5% lidocaine Cream

Manufacturer
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Effective date
2026-08-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-27 00:01:56

Label at a glance#

ProductLidocaine Numbing Cream
Active ingredientLIDOCAINE
Label structure14 sections

Indications and uses

For the temporary relief of local and anorectal itching and discomfort associated with hemorrhoids and other anorectal disorders. For the temporary relief of pain, soreness and burning.

Dosage and administration

Adults and children 12 years of age and over: ·when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly ·gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product ·Apply externally to the affected area up to 6 times daily Children under 12 years of age : consult a doctor

Storage and handling

·store at USP controlled room temperature 20°-25°C (68°-77°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5% ......................................... Local anesthetic

Purpose

OTC - PURPOSE SECTION

Local anesthetic

Uses

INDICATIONS & USAGE SECTION

  • For the temporary relief of local and anorectal itching and discomfort associated with hemorrhoids and other anorectal disorders.
  • For the temporary relief of pain, soreness and burning.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

·do not exceed the recommended daily 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 ... if

OTC - STOP USE SECTION

·bleeding occurs

·condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

·Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor promptly.

... ask a doctor if

OTC - ASK DOCTOR SECTION

·bleeding occurs

·condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding,

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:

·when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly

·gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product

·Apply externally to the affected area up to 6 times daily

Children under 12 years of age: consult a doctor

Other information

STORAGE AND HANDLING SECTION

·store at USP controlled room temperature 20°-25°C (68°-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Extract, Arnica Montana Flower Extract, Carbomer,Cetostearyl Alcohol, C10-18 Triglycerides, Dimethicone, Edetate Disodium, Ethylhexylglycerin, Glyceryl Mono- and Dipalmitostearate,Hydroxyacetophenone, Isopropyl Myristate, Polysorbate 60, Propylene Glycol, Vitamin E, Water

Questions or Comments:

OTC - QUESTIONS SECTION

86-21-31166566

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

311-49311-49311-36311-36

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136924239707605GTIN-13: 6924239707605
EAN-13: 6924239707605
GTIN storage (14 digits): 06924239707605
311-49.jpg

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73557-31173557-311-36, 73557-311-49

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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 Numbing CreamLIDOCAINEShanghai Chuangshi Medical Technology (Group) Co., Ltd.599b425a-0e96-76df-e063-6394a90a48ff2026-08-21WarningsExact identifier
ndc (package): 73557-311-49
ndc (package): 73557-311-36
ndc (product): 73557-311
ndc11 (package): 73557031149
ndc11 (package): 73557031136
spl id: 599b41ca-6965-76d8-e063-6394a90abe76
spl set id: 599b425a-0e96-76df-e063-6394a90a48ff

Reported adverse events (FAERS/openFDA)#

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