CVS PHARMACY MAXIMUM STRENGTH FEMININE WIPES- pramoxine hydrochloride cloth

CVS Pharmacy by

Drug Labeling and Warnings

CVS Pharmacy by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Guy & O'Neill, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Pramoxine Hydrochloride 1.0% w/w

Purpose

ANALGESIC

Uses

• Temporarily relieves itching

Warnings

For external use only

When using this product

• Avoid contact with eyes

Stop use and ask a doctor if

• Condition worsens or does not improve within 7 days or clears up and reoccurs within a few days

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Direction

• Adults: unfold wipe and cleanse the area by gently wiping or patting external vaginal area from front to back. Use each towel only once and discard.
• Use up to 4 times daily.
• Children under 12: consult a doctor

Other information

• Store at room temperature
• Discard within 2 months of opening

Inactive ingredients

purified water, glycerin, propylene glycol, cocoamphodiacetate, polysorbate 20, aloe vera barbadensis leaf juice, citric acid, fragrance, diazolidinyl urea, iodopropynyl butylcarbamate.

Questions or comments?

Call weekdays 8am-5pm CST 1-800-325-5358

Images of representative packaging

CVSFemWipesBox.jpgCVSFemWipesLabel.jpg CVSFemWipesDrugFactsPanel.jpg

INGREDIENTS AND APPEARANCE

CVS PHARMACY  MAXIMUM STRENGTH FEMININE WIPES
pramoxine hydrochloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-993
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-993-01	89 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	03/21/2013

Labeler - CVS Pharmacy (062312574)

Registrant - Guy & O'Neill, Inc. (962567264)

Establishment
Name	Address	ID/FEI	Business Operations
Guy & O'Neill, Inc.		037838844	manufacture(59779-993)