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Nupharmisto Tattoo Numbing Cream

Dosage form
CREAM
Labeler
Ehy Holdings LLC
Label updated
2023-02-15
Retrieved
2026-09-07
Active ingredients
LIDOCAINE
View original label and images on DailyMed ↗
Active Ingredient(s)

Lidocaine 5%

Purpose

Local Anesthetic

Use

For the temporary relief of local and anorectal discomfort associated with anorectal disorder or inflammation.

Warnings

For external use only

Do not use

Pregnant or breastfeeding, ask a health professional before use.
In case of accidental overdose, get medical help or contact the
Poison Control Center immediately.
Seal is broken or missing

Label information

directed by a doctor.
certain persons can develop allergic reactions to ingredients
in this product.
do not put this product into the rectum by using finger or
any medical device or applicator

Label information

the symptom being treated does not subside, or if redness

Label information

Adults: When practical, cleanse the affected area with mild soap
and warm water and rise thoroughly.
Gently dry by patting with toilet tissue or a soft cloth, before
application of this product.
Apply up to 6 times a day.
Children under 12 years of age: consult a doctor

Directions

Adults: When practical, cleanse the affected area with mild soap
and warm water and rise thoroughly.
Gently dry by patting with toilet tissue or a soft cloth, before
application of this product.
Apply up to 6 times a day.
Children under 12 years of age: consult a doctor

Other information

Keep away from direct sunlight or heat.
Store at room tempetature 15°-30°C (59°-86°F)

Inactive ingredients

Carbomer 934, Emu Oil, Arnica, Lecithin(Soybean), Propylene
Glycol, Tocopheryl Acetate, Benzyl Alcohol, Water

Label information

irritation, swelling, pain, or other symptoms develop or increase

제조사 문의
Package Label - Principal Display Panel

81799-008-01 1

[Image in the official label — see DailyMed source]

81799-008-01 2

[Image in the official label — see DailyMed source]

DailyMed Set ID: f4be3cb8-7015-1b65-e053-2995a90a3955 · Version 1
NDC: 81799-008