Bikini Zone Medicated CREME

Dosage form: cream
Ingredients: LIDOCAINE 2g in 100g
Labeler: CCA Industries, Inc.
NDC code: 61543-1601

Medically reviewed by Drugs.com. Last updated on Mar 11, 2024.

Bikini Zone Medicated CREME

Drug Facts

Active Ingredient

LIDOCAINE 2.00%

Purpose

topical analgesic/anesthetic

Use

temporarily relieves pain and itching associated with minor skin irritation.

Warnings

For external use only.

Avoid contact with eyes

Do not use

in large quantities, particularly over raw surfaces or blistered areas.
before any hair removal process that involves heat or lasers

Stop use and ask a doctor if

Condition worsens
Symptoms last for more than 7 days or clear up and occur again within a few days.
redness is present
irritation develops

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

adults and children 12 years and older

see top of cap to open tube
immediately after hair removal, apply sparingly to areas affected
repeat as necessary, but no more than 4 times daily
continue to apply as a part of your hair removal routine, whether you use a razor, wax or depilatory.
children under 2 years: ask a doctor

Other information

store at room temperature 15°-30°C (59°-86°F)

Inactive Ingredients

aloe barbadensis gel, benzyl alcohol, camphor, cetearyl alcohol, cyclohexasiloxane, cyclopentasiloxane, disodium edta, diazolidinyl urea, fragrance, glyceryl dilaurate, glyceryl stearate, hexylene glycol, lactic acid, menthol, methylparaben, octyldodecanol, peg-40 stearate, peg-100 stearate, polyquaternium-37, ppg-1 trideceth-6, propylene glycol dicaprylate/dicaprate, propylene glycol, propylparaben, salicylic acid, sd alcohol 23a, sodium hydroxide, water (aqua).

Questions or Comments?

Call 1-800-595-6230

Package Labeling:

BIKINI ZONE MEDICATED CREME
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:61543-1601
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (LIDOCAINE)	LIDOCAINE	2 g in 100 g

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL
CAMPHOR (NATURAL)
CETOSTEARYL ALCOHOL
CYCLOMETHICONE 6
CYCLOMETHICONE 5
EDETATE DISODIUM
DIAZOLIDINYL UREA
GLYCERYL MONOSTEARATE
HEXYLENE GLYCOL
LACTIC ACID
MENTHOL
METHYLPARABEN
OCTYLDODECANOL
POLYOXYL 100 STEARATE
PROPYLENE GLYCOL DICAPRYLATE
PROPYLENE GLYCOL
PROPYLPARABEN
SALICYLIC ACID
SODIUM HYDROXIDE
WATER

Packaging
#	Item Code	Package Description
1	NDC:61543-1601-1	1 TUBE in 1 BOX
1		28 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	06/03/2010

Labeler - CCA Industries, Inc. (106771041)

Revised: 03/2019

Document Id: 848d7654-d18b-1d88-e053-2a91aa0ad5a5

Set id: 091169e6-5021-431e-ab68-8c10e4f8f0c5

Version: 6

Effective Time: 20190320

CCA Industries, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer