FDA.reportPublic FDA data

Walgreens Moisture Barrier

Product NDC
0363-3680
11-digit product format
003633680
Labeler code
0363
Product ID
0363-3680_48644572-85a9-bf56-e063-6294a90a2534
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol, and Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Walgreen Company
Application
M015
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2015-02-16
Substance
MENTHOL; ZINC OXIDE
Active strength
.44; 20.6 g/100g; g/100g
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage0363-3680-04fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage0363-3680-0486f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage0363-3680-04bd6a592717d7…303034d00443…

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
Walgreens Moisture Barrier
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL.44 g/100g
ZINC OXIDE20.6 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L7T10EIP3AInternal UNII lookup
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
a6db6f13-4e02-47dc-aef6-a804506c3d8bAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-3680-042024-02-06C16284748780-1d6a99b39-4e96-a426-e053-dadaa90af4c2Walgreens Moisture Barrier Ointment 4 oz NBE Calmoseptine
0363-3680-042022-01-28C16284748780-1d6a99b39-4e96-a426-e053-dadaa90af4c2Walgreens Moisture Barrier Ointment 4 oz NBE Calmoseptine

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-3680-04Walgreens Moisture Barrier113 g in 1 TUBECREAM1136
0363-3680-04Walgreens Moisture Barrier1 in 1 PACKAGECREAM16

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-3680-04GM - Gram0363-3680e9a100ea-7909-4cd8-9923-abe9004e7b6c12020-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3AWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54ZWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
MENTHOLACTIVE MOIETYL7T10EIP3AWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
ZINC CATIONACTIVE MOIETY13S1S8SF37WALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
ERGOCALCIFEROLINACTIVE INGREDIENTVS041H42XCWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
LANOLININACTIVE INGREDIENT7EV65EAW6HWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
PARAFFININACTIVE INGREDIENTI9O0E3H2ZEWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
PETROLATUMINACTIVE INGREDIENT4T6H12BN9UWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
PHENOLINACTIVE INGREDIENT339NCG44TVWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
POLYSORBATE 60INACTIVE INGREDIENTCAL22UVI4MWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1
WATERINACTIVE INGREDIENT059QF0KO0RWALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-3680WALGREENS MOISTURE BARRIER (MENTHOL, AND ZINC OXIDE) CREAM [WALGREEN COMPANY]5Current NDC, Legacy NDC, 2 package rows20241227_a6db6f13-4e02-47dc-aef6-a804506c3d8b.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 11 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MedlineMENTHOL, WHITE PETROLATUM, ZINC OXIDEMedline Industries, LP006539c9-1982-d6de-e063-6294a90a1a5a2025-10-17WarningsExact identifier
application number: M015
Xesso Strawberry Rear Comfort Glide 4% LidocaineLIDOCAINEPremium Natural Cosmetics Incefba09fc-6dd7-0f73-e053-2995a90a628a2025-10-17WarningsExact identifier
application number: M015
medicated padsWITCH HAZELTARGET CORPORATIONacd0d99d-2a77-4227-bebb-c819f4a526662025-10-14WarningsExact identifier
application number: M015
Acolye Numbing Cream Anorectal(Hemorrhoidal) CreamLIDOCAINEGuangzhou Haishi Biological Technology Co., Ltd.40b0e8d6-4686-960b-e063-6294a90a016e2025-10-09WarningsExact identifier
application number: M015
Acolye Numbing Cream Anorectal(Hemorrhoidal) CreamLIDOCAINEGuangzhou Haishi Biological Technology Co., Ltd.40b452a3-76b7-2433-e063-6294a90ab6b42025-10-09WarningsExact identifier
application number: M015
EQUATE HEMORRHOID RELIEFLIDOCAIN 5%WALMART, INCd96e8152-e36e-22fc-e053-2995a90a8b2b2025-10-08WarningsExact identifier
application number: M015
Pramoxine Hydrochloride AnorectalPRAMOXINE HYDROCHLORIDEStratus Pharmaceuticals39a16b66-b0e9-412f-8773-8dec0a1227e02025-10-02WarningsExact identifier
application number: M015
Doctor Butlers Hemorrhoid and Fissure External Pain FormulaLIDOCAINE 5%Beyond Health, P.A.d92f22a7-c0b5-d8b8-e053-2a95a90a23762025-09-30WarningsExact identifier
application number: M015
RWWXII Deep Numbing Cream(Anorectal Hemorrhoidal Cream)LIDOCAINEGuangzhou Haishi Biological Technology Co., Ltd.3ffc57c7-5bf4-cba8-e063-6394a90a322f2025-09-29WarningsExact identifier
application number: M015
Hemorrhoidal Pain ReliefHEMORRHOIDAL PAIN RELIEF CREAMNeilmed Pharmaceuticals Inc.374dc1c0-4243-b272-e063-6394a90a5a6b2025-09-24WarningsExact identifier
application number: M015
Medi-First BurnLIDOCAINE HYDROCHLORIDEUnifirst First Aid Corporation44bb5f25-1114-4bb1-8bcf-40402594abc42025-09-09WarningsExact identifier
application number: M015
Dr. Care Numbing Cream5% LIDOCAINEShengnan (Guangzhou) Cosmetics Co., LTD3e456af7-9726-d17e-e063-6394a90ab5602025-09-08WarningsExact identifier
application number: M015
Medi-first Ivy-Rid First AidBENZOCAINE AND BENZETHONIUM CHLORIDEUnifirst First Aid Corporation905c97ad-0bba-46b1-939c-f16fbdb028182025-09-08WarningsExact identifier
application number: M015
MediFirst BurnLIDOCAINE HYDROCHLORIDEUnifirst First Aid Corporation9fa5b348-29c2-4cd0-a945-0486bd27f5e02025-09-08WarningsExact identifier
application number: M015
Medi-First BurnLIDOCAINE HCLUnifirst First Aid Corporationb3ebf104-cc51-0ef5-e053-2a95a90a25c92025-09-08WarningsExact identifier
application number: M015
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEUnifirst First Aid Corporation4c2e2b91-d2f6-4e41-9a4c-ecabca9830e82025-09-08WarningsExact identifier
application number: M015
Pain ReliefANALGESIC MENTHOLUnifirst First Aid Corporation8162d22d-04c0-de07-e053-2991aa0a99752025-09-08WarningsExact identifier
application number: M015
Green Guard BurnLIDOCAINE HCLUnifirst First Aid Corporationb451e96f-fcba-6495-e053-2a95a90a2adf2025-09-08WarningsExact identifier
application number: M015
Lidochill(TM) GelLIDOCAINE HCL 4%, MENTHOL 1%PureTek Corporationd2a9aeb6-8a94-49e7-ab46-84403560b6c82025-09-08WarningsExact identifier
application number: M015
Signature numbing cream5% LIDOCAINEShengnan (Guangzhou) Cosmetics Co., LTD3e1892de-378b-d2d0-e063-6294a90ad7db2025-09-05WarningsExact identifier
application number: M015

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-3680-04003633680041 TUBE in 1 PACKAGE (0363-3680-04) / 113 g in 1 TUBE1 tube2016-10-040000-00-00NoNoCurrent