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Critic Aid Clear AF

Coloplast Manufacturing US, LLC
Coloplast Corp

Antifungal OintmentClear Moisture Barrier With Antifungal




FULL PRESCRIBING INFORMATION

For Perineal
Skin Irritation Due To
Fungal Infection

  • Adheres to denuded skin
  • Easy to apply and remove
  • Treats topical fungal infections

Drug Facts

Active ingredient

Active ingredient

Miconazole nitrate, 2%

Purpose

Purpose

Antifungal

Uses

Uses For effective treatment of jock itch. Relieves itching, scaling, irritation, redness and discomfort.

Warnings

When using this product

  • avoid contact with eyes
  • do not use on children under 2 years of age unless directed by a doctor

Stop using this product and ask a doctor if irritation occurs or there is no improvement within 2 weeks.

For external use only. Keep this and all drugs out of the 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 thin layer of product over affected area twice daily (morning and night), or as directed by a doctor
  • supervise children in the use of this product.

Use daily for 2 weeks.

If condition persists, consult a doctor. This product is not effective on scalp or nails.

Inactive ingredients

cellulose gum, dimethicone, petrolatum, tocopheryl acetate

Patent Pending

See crimp for lot no. and expiration date

Manufactured by: Coloplast A/S DK-3050 Humlebaek, Denmark
Distributed by: Coloplast Corp. Minneapolis, MN 55411 U.S.A.
1-800-533-0464 www.us.coloplast.com Product #7572
©2007, Coloplast Corp. Made in the U.S.A.

L7-1349

PRINCIPAL DISPLAY PANEL - NET WT. 5 OZ. (142g)

NDC 11701-067-14

Critic-Aid ® Clear AF

Antifungal Ointment

Clear Moisture Barrier With Antifungal

For Perineal

Skin Irritation Due To

Fungal Infection

Coloplast

NET WT. 5 OZ. (142 g)

Critic Aid Clear AF

Miconazole Nitrate OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11701-067
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE 20 mg

Inactive Ingredients

Ingredient Name Strength
petrolatum
.ALPHA.-TOCOPHEROL ACETATE, D-
DIMETHICONE
CROSCARMELLOSE SODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11701-067-22 4 in 1 PACKET
2 NDC:11701-067-23 57 in 1 TUBE
3 NDC:11701-067-14 142 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2009-06-15


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