PUTRIZEN 40 UREA

Product NDC
84989-025
11-digit product format
849890025
Labeler code
84989
Product ID
84989-025_533dadbc-6f21-d880-e063-6394a90a753f
Type
HUMAN OTC DRUG
Nonproprietary name
GLYCERIN
Dosage form
CREAM
Route
TOPICAL
Labeler
Shantou Ximonth Biotechnology Co., Ltd.
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-06-02
Substance
BUTYROSPERMUM PARKII (SHEA) BUTTER; SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL; MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
Active strength
12; 7.5; .3 mg/150mg; mg/150mg; mg/150mg
NDC exclude flag
No
Listing certified through
2027-12-31
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
PUTRIZEN 40 UREA
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BUTYROSPERMUM PARKII (SHEA) BUTTER12 mg/150mg
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL7.5 mg/150mg
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL.3 mg/150mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
K49155WL9YInternal UNII lookup
724GKU717MInternal UNII lookup
VIF565UC2GInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
533dadbc-6f20-d880-e063-6394a90a753fAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

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 25 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Kenkoderm Eczema Honey Soothing BodyKENKODERM ECZEMA HONEY SOOTHING BODY LOTIONGuangzhou Ariel Biotech Co., Ltd.4865c697-05fc-eac8-e063-6294a90ae5412026-01-14WarningsExact identifier
application number: M016
Gold Bond Medicated eczema reliefCOLLOIDAL OATMEALChattem, Inc.52744c77-278f-40b1-a356-14ae4366389b2026-01-14WarningsExact identifier
application number: M016
Water Drench Hyaluronic Healing BalmDIMETHICONEPeter Thomas Roth Labs, LLC3f789176-1d80-d146-e063-6294a90a948a2026-01-13WarningsExact identifier
application number: M016
DERMEDIAL Anti-ItchOATMEAL, ZINC OXIDESaje Natural Business Inc385dd757-740b-8324-e063-6294a90afeee2026-01-13WarningsExact identifier
application number: M016
Sweet cheeksZINC OXIDESaje Natural Business Inc.5fc6486e-8604-5c7b-e053-2991aa0a8d142026-01-13WarningsExact identifier
application number: M016
TeevodarALLANTOINPEER PHARM LTD.57a1b6d1-9439-462b-aeb9-ef806e572eaf2026-01-12WarningsExact identifier
application number: M016
Botao Baby Diaper Rash CreamZINC OXIDEPeer Pharm Ltd.df60a70e-e6c0-41b3-e053-2995a90af1762026-01-12WarningsExact identifier
application number: M016
ECZEMA HAND RELIEFCOLLOIDAL OATMEALSkinfix, Inc.0389bab7-04fb-7cfc-e063-6394a90a22d82026-01-12WarningsExact identifier
application number: M016
SKINFIX HAND REPAIROATMEALSkinfix, Inc.1b65fc81-1b9e-4260-829a-332cf6891d022026-01-12WarningsExact identifier
application number: M016
ECZEMA INTENSIVE DAILY RELIEF BODYCOLLOIDAL OATMEAL CREAMSkinfix, Inc.0be3c631-bc9b-00a9-e063-6394a90abcbb2026-01-12WarningsExact identifier
application number: M016
SarnaCOLLOIDAL OATMEALCrown Laboratories, Inc.2d6b1872-9f4d-9eb3-e063-6394a90ab6752026-01-12WarningsExact identifier
application number: M016
XIMONTH Nail Repairs PatchesGLYCERINShantou Ximonth Biotechnology Co., Ltd.47f1a711-5d6f-c023-e063-6294a90aa8012026-01-09WarningsExact identifier
application number: M016
Endit zinc oxide skin protectionZINC OXIDEEndIt Laboratories, Inc.e60bb0da-3349-f8f9-e053-2a95a90a90512026-01-09WarningsExact identifier
application number: M016
Endit Zinc Oxide Skin ProtectantZINC OXIDEEndit Laboratories, Inc.55b3aa07-871d-421b-b76a-c2d359d6003f2026-01-09WarningsExact identifier
application number: M016
Flanders ButtocksWHITE PETROLATUM, ZINC OXIDEFlanders Inc32371159-c76d-41b0-e054-00144ff88e882026-01-09WarningsExact identifier
application number: M016
Pure Petrolatum JellyPETROLATUMMY IMPORTS USA LLC47da77ea-ab4e-fc3c-e063-6394a90a27b72026-01-08WarningsExact identifier
application number: M016
Z-BumDIAPER RASH CREAMGM Pharmaceuticals, Inc2a36f396-3a30-3f3f-e054-00144ff8d46c2026-01-08WarningsExact identifier
application number: M016
Daily VLotionDIMETHICONEKindra1cc4b804-6483-68fd-e063-6294a90a38e42026-01-08WarningsExact identifier
application number: M016
V Relief SerumDIMETHICONEKindra1cd8a9e9-ac88-1799-e063-6294a90a32782026-01-08WarningsExact identifier
application number: M016
DR SMITHS DIAPERZINC OXIDEMission Pharmacal7705b182-acf7-4195-9996-7d9fcdfbf0552026-01-08WarningsExact identifier
application number: M016

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84989-025-0184989002501150 mg in 1 BOTTLE, PLASTIC (84989-025-01) 150 mg2026-06-02NoNoCurrent