Other
Numb Cream
Numb Cream
FDA Label NDC 84019-301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shengnan (guangzhou) Cosmetics Co., Ltd for the product Numb Cream (NDC 84019-301). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
LIDOCAINE 4%
Otc - Purpose
Topical Analgesic
Indications & Usage
For temporarily relieve local discomfort, itching, pain, soreness or burning sensation on hands, legs, back and other skin.
Warnings
For external use only
Otc - Do Not Use
lf pregnant or breast-feeding, ask a health professional before use.
Otc - When Using
Use only as directed.
Avoid contact with the eyes,
mucous membranes, or rashes.
Do not bandage tightly.
Otc - Stop Use
skin reactions such as redness.swelling, blistering or other discomfort occur.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
lf swallowed accidentally, get medical help or contact with Poison Control Center immediately.
Dosage & Administration
1.For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly.
2.Apply externally to the affected area up to 6 times.
Inactive Ingredient
Water
Propylene Glycol
Carbomer
Glycerin
Disodium Edta
Hydroxyacetophenone
1.2-Hexanediol
Mentha Arvensis Leaf Extract
Chrysanthellum Indicum Extract
Portulaca Oleracea Extract
Peg-40 Hydrogenated Castor Oil
Epinephrine
Tetracaine
Prilocaine
Borneol
Package Label.Principal Display Panel
Label1 (Label 1)
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