Label: CRITIC AID CLEAR- petrolatum ointment
- NDC Code(s): 11701-066-22, 11701-066-32, 11701-066-33
- Packager: Coloplast Manufacturing US, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients
cellulose gum, dimethicone, tocopheryl acetate, zinc oxide
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 #7567
©2007, Coloplast Corp. Made in the U.S.A.E10-1347
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CRITIC AID CLEAR
petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11701-066 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 710 mg in 1 g Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) DIMETHICONE (UNII: 92RU3N3Y1O) ZINC OXIDE (UNII: SOI2LOH54Z) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11701-066-22 4 g in 1 PACKET; Type 0: Not a Combination Product 06/15/2009 2 NDC:11701-066-33 71 g in 1 TUBE; Type 0: Not a Combination Product 06/15/2009 3 NDC:11701-066-32 170 g in 1 TUBE; Type 0: Not a Combination Product 06/15/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M016 06/15/2009 Labeler - Coloplast Manufacturing US, LLC (110326675) Registrant - Coloplast Corp (847436391) Establishment Name Address ID/FEI Business Operations Coloplast Manufacturing US, LLC 110326675 MANUFACTURE(11701-066)