Label: BAZA CLEAR- petrolatum ointment
- NDC Code(s): 11701-048-14, 11701-048-22, 11701-048-24
- Packager: Coloplast Manufacturing US, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
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SPL UNCLASSIFIED SECTION
Drug Facts
Uses Helps treat and prevent minor skin irritation due to diaper rash. Helps prevent and temporarily protects chafed, chapped or cracked skin. Helps seal out wetness.
When using this product
- avoid contact with eyes
- not to be applied over deep or puncture wounds or lacerations.
Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- apply liberally as often as necessary.
For Diaper Rash: cleanse the diaper area and allow to dry
- apply liberally as often as necessary, with each diaper change especially at bedtime or any time when exposure to wet diapers may be prolonged.
Inactive ingredients benzethonium chloride, BHT, cod liver oil, fragrance, green 6, sodium caseinate (CONTAINS MILK)
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 #1006 ©2008-7, Coloplast Corp.
Made in the U.S.A.G8-303
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BAZA CLEAR
petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11701-048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 960 mg in 1 g Inactive Ingredients Ingredient Name Strength COD LIVER OIL (UNII: BBL281NWFG) SODIUM CASEINATE (UNII: 7473P66J9E) BENZETHONIUM CHLORIDE (UNII: PH41D05744) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) D&C GREEN NO. 6 (UNII: 4QP5U84YF7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11701-048-22 4 g in 1 PACKET; Type 0: Not a Combination Product 06/15/2009 2 NDC:11701-048-24 50 g in 1 TUBE; Type 0: Not a Combination Product 06/15/2009 3 NDC:11701-048-14 142 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(11701-048)
