CVS HEALTH MAXIMUM STRENGTH FEMININE- pramoxine hydrochloride cloth

CVS Health Maximum Strength Feminine by

Drug Labeling and Warnings

CVS Health Maximum Strength Feminine by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                              Purpose

Pramoxine hydrochloride 1% w/w......................................Extnernal analgesic

PURPOSE

Use

temporarily relieves itching

WARNINGS

Warnings

For external use only

Avoid contact with eyes

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Directions

Adults and children 12 years of age and older: Unfold towellete and gently pat or wipes external vaginal area from front to back. Use each towelette only once and then throw away. Apply to affected area not more than 3 to 4 times daily.

Children under 12 years of age: Consult a doctor.

STORAGE AND HANDLING

Other information

• store at room temperature
• discard within 2 months of opening

INACTIVE INGREDIENT

Inactive ingredients

water, glycerin, phenoxyethanol, polyaminopropyl biguanide, polysorbate 20, sodium methylparaben, fragrance, benzoic acid, disodium cocamphodiacetate, dehydroacetic acid, aloe barbadensis leaf juice powder, toceopheryl acetate

DOSAGE & ADMINISTRATION

Distributed by:

CVS Pharmacy, Inc.

Once CVS Drive,

Woonsocket, RI 02895

CVS.com 1-800-SHOP CVS

Made in China

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS HEALTH MAXIMUM STRENGTH FEMININE 
pramoxine hydrochloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-128
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM (UNII: 9NEZ333N27)
METHYLPARABEN (UNII: A2I8C7HI9T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-128-20	20 in 1 POUCH; Type 0: Not a Combination Product	01/26/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	01/26/2017

Labeler - CVS Pharmacy (062312574)