Tattoo Numbing Cream

Manufacturer
Sainite Trading Shenzhen Co., Ltd.
Effective date
2022-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:55:37

Label at a glance#

ProductTattoo Numbing Cream
Active ingredientLIDOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

OTC - PURPOSE SECTION

Topical anesthetic

INSTRUCTIONS FOR USE SECTION

For temporary relief of local discomfort, itching, pain, soreness.

WARNINGS SECTION

For external use only. Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days. When using this product avoid contact with eyes. Flush with water if contact occurs. Do not apply over large areas of the body, particularly over raw surfaces or blistered areas.

OTC - DO NOT USE SECTION

Pregnant or breastfeeding, ask a health professional before use.

INACTIVE INGREDIENT SECTION

Aloe barbadebsis leaf juice (Aloe vera), Water, Lecithin (Soybean), PropyleneGlycol, Tocopheryl Acetate, Carbomer, Menthol, Triethanolamine.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

• When practical, clean area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet
tissue or soft cloth before applying.
• Adults and children 12 years and older: apply externally to the affected area up to 6 times a day.
• Children under 12 years of age: consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older: For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product.

Apply externally up to 6 times per day.

Children under 12: Consult a Doctor.

OTHER SAFETY INFORMATION

Keep away from direct sunlight or heat
Store in room temperature (59-86°F/15-30°C)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10ml label10ml labelNDC: 82929-012-08 10ml in 1 Tube

NDC: 82929-012-09 40ml in 1 Tube

40ml label40ml label

NDC: 82929-012-10 60ml in 1 Tube

60ml label60ml label

Products#

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DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82929-01282929-012-08, 82929-012-09, 82929-012-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
e607c219-94da-503b-e053-2a95a90aad27e607c219-94d9-503b-e053-2a95a90aad272022-08-12WarningsExact identifier
spl id: e607c219-94da-503b-e053-2a95a90aad27
spl set id: e607c219-94d9-503b-e053-2a95a90aad27

Reported adverse events (FAERS/openFDA)#

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