CRITIC AID CLEAR- petrolatum ointment 
Coloplast Manufacturing US, LLC

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Critic-Aid®Clear
Skin Protectant
Clear Moisture Barrier Ointment

For Minor To Severe
Skin Irritation
Due To Incontinence

Drug Facts

Active ingredient

Petrolatum, 71.5%

Purpose

Diaper Rash Skin Protectant

Uses Helps treat and prevent minor skin irritation due to diaper rash. Helps seal out wetness.

Warnings

When using this product

  • avoid contact with eyes
  • not to be applied over deep or puncture wounds or lacerations.

Consult a doctor

  • if condition worsens or does not improve within 7 days.

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

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 - NET WT. 6 OZ. (170 g)

NDC 11701-066-32

Critic-Aid®Clear

Skin Protectant

Clear Moisture Barrier Ointment

For Minor To Severe

Skin Irritation

Due To Incontinence

Coloplast

NET WT. 6 OZ. (170 g)

PRINCIPAL DISPLAY PANEL - NET WT. 6 OZ. (170 g)
CRITIC AID CLEAR 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11701-066
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM710 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11701-066-224 g in 1 PACKET; Type 0: Not a Combination Product06/15/2009
2NDC:11701-066-3371 g in 1 TUBE; Type 0: Not a Combination Product06/15/2009
3NDC:11701-066-32170 g in 1 TUBE; Type 0: Not a Combination Product06/15/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM01606/15/2009
Labeler - Coloplast Manufacturing US, LLC (110326675)
Registrant - Coloplast Corp (847436391)
Establishment
NameAddressID/FEIBusiness Operations
Coloplast Manufacturing US, LLC110326675MANUFACTURE(11701-066)

Revised: 12/2023
Document Id: cae3b046-d152-4c35-9103-4a239381bfde
Set id: 0b6da97e-519b-4579-9895-f4ede5c48b47
Version: 6
Effective Time: 20231221
 
Coloplast Manufacturing US, LLC