Label: BAZA CLEANSE AND PROTECT ODOR CONTROL- dimethicone lotion
- NDC Code(s): 11701-062-05
- Packager: Coloplast Manufacturing US, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 21, 2023
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Drug Facts
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 the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- change wet and soiled diapers promptly
- spray affected area and gently wipe with clean, soft cloth
- apply as often as necessary, with each diaper change, especially at bedtime or any time when exposure to wet diapers may be prolonged.
Inactive ingredients allantoin, cetearyl alcohol, citric acid, diazolidinyl urea, fragrance, glycerin, glyceryl stearate, isopropyl palmitate, metfiylparaben, panthenol, propylene glycol, propylparaben, sodium laurovl lactvlate. soybean oil. tocoDhervl acetate (vitamin B. water, zinc ricinoleate
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 #7725
©2008-9, Coloplast Corp. Made in the U.S.AJ8-1222
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BAZA CLEANSE AND PROTECT ODOR CONTROL
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11701-062 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) SOYBEAN OIL (UNII: 241ATL177A) ZINC RICINOLEATE (UNII: BOH1Z111J2) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PANTHENOL (UNII: WV9CM0O67Z) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) ALLANTOIN (UNII: 344S277G0Z) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11701-062-05 227 g in 1 BOTTLE; 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(11701-062)