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CVS Feminine Intimate Powder

Medically reviewed by Drugs.com. Last updated on Mar 27, 2020.

Dosage form: powder
Ingredients: MICONAZOLE NITRATE 20mg in 1g
Labeler: PureTek Corporation
NDC Code: 59088-244

Drug Facts

Active ingredient
Miconazole Nitrate 2%

Purposes

Antifungal 

Uses
  • for the treatment and relief of external genital itching
  • relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort and chafing associated with external genital itching

Warnings

For external use only

Do not use on children under 2 years of age unless directed by a doctor.

When using this product avoid contact with the eyes.

Stop use and ask a doctor if
  • irritation occurs or if there is no improvement within 2 weeks

Keep out of reach of children.

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

Directions
  • clean the affected area and dry thoroughly 
  • apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor 
  • supervise children in the use of this product 

Other information
  • store between 59°-86°F
  • lightly shake bottle to loosen settled powder

Inactive ingredients

Aleurites Moluccana Seed Oil, Aloe Barbadensis (Aloe Vera) Leaf Juice Powder, Bisabolol, Carthamus Tinctorius (Safflower) Oleosomes, Fragrance, Nylon-12, Silica, Sodium Benzoate, Sodium Hyaluronate, Zea Mays (Corn) Starch, Zingiber Officinale (Ginger) Root Extract.

CVS FEMININE INTIMATE POWDER 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-244
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (MICONAZOLE) MICONAZOLE NITRATE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
KUKUI NUT OIL 
ALOE VERA LEAF 
LEVOMENOL 
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES 
NYLON-12 
SILICON DIOXIDE 
SODIUM BENZOATE 
HYALURONATE SODIUM 
STARCH, CORN 
GINGER 
Packaging
#Item CodePackage Description
1NDC:59088-244-0785 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C05/31/2019
Labeler - PureTek Corporation (785961046)
Establishment
NameAddressID/FEIOperations
PureTek Corporation785961046manufacture(59088-244)

 
PureTek Corporation

Further information

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