Boudreauxs

Product NDC
0132-0334
11-digit product format
001320334
Labeler code
0132
Product ID
0132-0334_a0a6ee4a-fae8-4795-ab6f-c2470e9ed7c1
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
C.B. Fleet Company, Inc.
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-02-01
Substance
ZINC OXIDE
Active strength
16 g/113g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Boudreauxs
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE16 g/113g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
SOI2LOH54ZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
262278f6-7e4c-44ee-b40d-39662a239d73Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0132-0334-44Boudreauxs113 g in 1 TUBECREAM1137

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0132-0334BOUDREAUXS (ZINC OXIDE) CREAM [C.B. FLEET COMPANY, INC.]6Current NDC, Legacy NDC, 1 package rows20240704_262278f6-7e4c-44ee-b40d-39662a239d73.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 30 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
First Aid Beauty FAB Ultra Repair Skin Protectant Chai CinnamonCOLLOIDAL OATMEALThe Procter & Gamble Manufacturing Company4576cd28-9531-4db4-e063-6394a90a9fd32025-12-08WarningsExact identifier
application number: M016
First Aid Beauty FAB Ultra Repair Skin ProtectantCOLLOIDAL OATMEALThe Procter & Gamble Manufacturing Companybeb22d69-8a83-65dc-e053-2a95a90ad8122025-12-08WarningsExact identifier
application number: M016
Medicated Hemorrhoidal PadsWITCH HAZELCardinal Health0b49db40-7abc-4e62-b6da-4b9f5b0ae16d2025-12-05WarningsExact identifier
application number: M016
CVS Health MedicatedWITCH HAZELCVS Pharmacya74ab253-cafc-4f00-9b8f-e5c1e6e7f2212025-12-05WarningsExact identifier
application number: M016
Major Medi-PadsWITCH HAZELMajor Pharmaceuticalsd2a314a2-98ab-4ac0-9e90-1a8c1303958f2025-12-05WarningsExact identifier
application number: M016
Good Sense MedicatedWITCH HAZELGeiss, Destin & Dunn, Inc5f122db5-4391-4957-9c25-76834c356c4f2025-12-05WarningsExact identifier
application number: M016
Witch HazelMEDICATED HEMORRHOIDAL WIPESGiant Eaglecdd9d6b7-cbc9-2839-e053-2a95a90ada002025-12-05WarningsExact identifier
application number: M016
Cool ComfortORGANIC WITCH HAZELNaticura Incde14c19c-56b5-4727-9194-94e85425ca8a2025-12-05WarningsExact identifier
application number: M016
GOODSENSE Maximum Strength MedicatedWITCH HAZELGEISS, DESTIN & DUNN, INC5453a12b-e775-4101-bd3a-337857e9e1672025-12-05WarningsExact identifier
application number: M016
Medicated Multipurpose WipesWITCH HAZELQUEST USA CORP.0f28d5f9-b20a-ac6f-e063-6394a90ac2082025-12-05WarningsExact identifier
application number: M016
Gold Bond Medicated eczema reliefCOLLOIDAL OATMEALGold Bond Co LLCc292e443-7418-4679-b9b2-4e6d96c04c4c2025-12-05WarningsExact identifier
application number: M016
Prequel Skin Utility OintMULTI PURPOSE SKIN PROTECTANTThe Center Brands, LLC2bf0931e-245d-14a6-e063-6294a90a66812025-12-04WarningsExact identifier
application number: M016
Prequel Skin Utility Balm Multi-Purpose Skin ProtectantSKIN PROTECTANT BALMThe Center Brands, LLC57c0b71d-6099-415c-976d-b96d2f73e9d32025-12-04WarningsExact identifier
application number: M016
Gold Bond Eczema Relief Medicated Skin Protectant CreamCOLLOIDAL OATMEALGold Bond Co LLC8fbbfde8-ead1-434f-ae23-6e69662638e12025-12-04WarningsExact identifier
application number: M016
Gold Bond Diabetics Dry Skin Relief Foot CreamDIMETHICONE AND WHITE PETROLATUMGold Bond Co LLC77b8c30b-d5ba-42ce-9313-4ce1b0bce8732025-12-04WarningsExact identifier
application number: M016
Gold Bond Eczema Relief Medicated Hand CreamCOLLOIDAL OATMEALGold Bond Co LLCb96e5deb-f2c7-421b-afac-bffb1c9b37ac2025-12-04WarningsExact identifier
application number: M016
UNIVERSAL PURE PETROLEUMWHITE PETROLEUMUniversal Distribution Center LLC6bc34bbe-e324-48f4-b6df-dd508b19c2e22025-12-03WarningsExact identifier
application number: M016
Calming Itch and IrritationCOLLOIDAL OATMEALBetter Planet Brands LLC1dd7e712-56a4-86c0-e063-6294a90a75cd2025-12-03WarningsExact identifier
application number: M016
Everyday EczemaCOLLOIDAL OATMEALBetter Planet Brands LLC1dd79ecf-5c5f-4888-e063-6394a90aff0f2025-12-03WarningsExact identifier
application number: M016
Scar Treatment BalmALLANTOINBetter Planet Brands LLC2cdc76f9-0044-fd07-e063-6294a90a680e2025-12-03WarningsExact identifier
application number: M016

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0132-0334-4400132033444113 g in 1 TUBE (0132-0334-44) 113 g2012-02-010000-00-00NoNoCurrent