Warnings
For external use only.
Dr. Care Numbing Cream
FDA Label NDC 84019-038
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 Dr. Care Numbing Cream (NDC 84019-038). 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 warnings, otc - purpose, otc - stop use, otc - active ingredient, otc - when using, inactive ingredient, dosage & administration, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Anorectal
(Hemorrhoidal)
Otc - Stop Use
Allergic reaction or
rectal bleeding occurs.
Redness, irritation,
swelling, or pain increases.
Condition worsens or
lasts >7 days
Otc - Active Ingredient
5% Lidocaine
Otc - When Using
Do not exceed daily
dose unless directed
by a doctor.
Do not insert into
rectum using fingers
or devices.
Inactive Ingredient
Water, Aleo vera
extract, Vitamin E,
Propylene Glycol,
Carbomer, Glycerin,
Disodium Edta,
Hydroxyacetophenone,
1,2-Hexanediol, Mentha
Arvensis Leaf Extract,
Chrysanthellum Indicum
Extract, Portulaca
Oleracea Extract.
Dosage & Administration
Adults and children 12
years and older: Apply a
thin layer to the affected
area 1-3 times daily or
as directed by a
healthcare provider.
Indications & Usage
Temporary relief of
pain, itching, soreness,
or burning in the
perianal area from
anorectal disorders.
Otc - Keep Out Of Reach Of Children
Keep out of reach of
children. If swallowed,
get medical help or call
Poison Control.
Package Label.Principal Display Panel
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