FDA.reportPublic FDA data

Numb Skin

Manufacturer
Seenext Venture Ltd
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:51:28

Label at a glance#

ProductNumb Skin
Active ingredientLIDOCAINE, BENZETHONIUM CHLORIDE
Label structure9 sections

Indications and uses

Can be used instead of soap and water to help clean minor cuts, scrapes, and burns For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, dermarolling, electrolysis, microblading, and piercing Temporarily relieves pain and itch while helping to prevent infection.

Dosage and administration

Use NumbSkin® Topical Anesthetic Foam Soap to cleanse the targeted area. Shake well before each use. Apply 2 to 3 pumps of foam soap andgently rub into the skin. Leave it onfor 5 to 10 minutes. Rinse off gentlywith running water or wipe with cleanpaper towel. Use before, during andafter the procedure. Make sure tocover the bottle tightly when not inuse, otherwise, the anesthetic effect will be lessened. Adults and...

Storage and handling

Store at controlled room temperature 59 0 ​-86 0 ​F (15 0 -30 0 C) Do not expose to temperature above 120 0 F(49 0 C) Protect from freezing

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

benzethonium Chloride 0.25%

Purpose

OTC - PURPOSE SECTION

External Analgesic and First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Can be used instead of soap and water to help clean minor cuts, scrapes, and burns
  • For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, dermarolling, electrolysis, microblading, and piercing
  • Temporarily relieves pain and itch while helping to prevent infection.

Warnings

WARNINGS SECTION

  • For external use only
  • avoid contact with eyes ​​

Do not use

OTC - DO NOT USE SECTION

  • do not use in large quantities particularly over raw surfaces or blistered area
  • do not exceed the recommended dosage unless directed by a doctor
  • in the eyes or apply over large areas of body
  • longer than one week unless directed by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds, animal bites or serious burns

Stop the use and consult doctor if:

OTC - STOP USE SECTION

  • condition worsenss or symptoms persist for more than 7 days or clear up and occur again within few days.

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

  • Use NumbSkin® Topical Anesthetic Foam Soap to cleanse the targeted area.
  • Shake well before each use.
  • Apply 2 to 3 pumps of foam soap andgently rub into the skin. Leave it onfor 5 to 10 minutes. Rinse off gentlywith running water or wipe with cleanpaper towel.
  • Use before, during andafter the procedure.
  • Make sure tocover the bottle tightly when not inuse, otherwise, the anesthetic effect will be lessened.

Adults and children two years old and older: Use to clean minor cuts, scrapes, and burns by thoroughly washing with water. Rinse and air dry. Use no more than three times daily.

Children under two years of age, ask a doctor.

Other information

STORAGE AND HANDLING SECTION

  • Store at controlled room temperature 59 0​-86 0​F (15 0-30 0C)
  • Do not expose to temperature above 120 0F(49 0C)
  • Protect from freezing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Benzyl Alcohol, Glycerin , Lauramidopropyl Betaine, Leuconostoc/Radish Root Ferment Filtrate, Menthoxypropanediol, Phenoxyethanol, Selaginella Lepidophylla Extract, Sodium Hydroxide, Water.

Question or comments?

OTC - QUESTIONS SECTION

Call weekdays 9 AM to 6 PM PST at 1-844-700- NUMB(6862) or email us at support@numbskin.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70907-002-50

NUMBSKIN

TOPICAL ANESTHETIC FOAM SOAP

4% LIDOCAINE

0.25% BENZETHONIUM CHLORIDE

DISINFECT NUMB SANITIZE

1.7 oz

LabelLabel

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70907-002-502024-01-30C16284748780-1ba0f9c33-2f58-a910-e053-dadaa90a0b85Drug Facts
70907-002-502022-01-17C16284748780-1ba0f9c33-2f58-a910-e053-dadaa90a0b85Drug Facts
70907-002-502021-01-29C16284748780-1ba0f9c33-2f58-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70907-002-50Numb Skin50 g in 1 TUBECREAM504
70907-002-50Numb Skin1 in 1 CARTRIDGECREAM14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70907-002NUMB SKIN (LIDOCAINE AND BENZETHONIUM CHLORIDE CREAM) CREAM [SEENEXT VENTURE LTD]4Legacy NDC, 2 package rows20221110_60389a84-7388-4604-a0f5-b69306959ba6.zip

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
70907-00270907-002-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
ALOE VERA LEAFZY81Z83H0XIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
BENZYL ALCOHOLLKG8494WBHIACT
GLYCERINPDC6A3C0OXIACT
LAURAMIDOPROPYL BETAINE23D6XVI233IACT
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
3-((L-MENTHYL)OXY)PROPANE-1,2-DIOLKD6TZ2QICHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SELAGINELLA LEPIDOPHYLLA02JQ564P1GIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
LIDOCAINE98PI200987ACTIB
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
ed0dd6c6-2a29-d5bb-e053-2995a90a33a860389a84-7388-4604-a0f5-b69306959ba62022-11-09WarningsExact identifier
spl id: ed0dd6c6-2a29-d5bb-e053-2995a90a33a8
spl set id: 60389a84-7388-4604-a0f5-b69306959ba6

Reported adverse events (FAERS/openFDA)#

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