NDC 85534-0102-01 - Olu Pain Management

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
85534-0102
Requested NDC
85534-0102-01
Package NDCs from labels
85534-0102-0, 85534-0102-1, 85534-0102-01
Manufacturer
HAWAII REPACK, INC.
Effective date
2026-08-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Olu Pain Management PatchHAWAII REPACK, INC.2026-08-28HUMAN OTC DRUG LABEL

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 314 of 346 · 6,908 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
XPRO Antiseptic Hand SanitizerALCOHOLSavone SAa62d427e-f332-f225-e053-2a95a90ab3872023-12-12WarningsExact identifier
unii: 3K9958V90M
TrubrexaLIDOCAINE AND CAPSAICINAsclemed USA, Inc.dbdf1df3-7289-4165-8815-f664bef82c562023-12-12WarningsExact identifier
unii: 98PI200987
ATTITUDE Super Leaves Hand Sanitizer Olive LeavesETHYL ALCOHOL9055-7588 Quebec Inc. DBA Attitude09d2fef3-00b3-9ee1-e063-6394a90ae3442023-12-11WarningsExact identifier
unii: 3K9958V90M
antiseptic hand sanitizer 01ALCOHOLCosmuses Cosmetics (Ningbo) Co., Ltd.e9f9b7b6-fed7-10e1-e053-2a95a90a9aa62023-12-11WarningsExact identifier
unii: 3K9958V90M
CVS Extra Strength Itch StoppingDIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATECVS857af609-9dd7-a07a-e053-2991aa0ab6ba2023-12-11WarningsExact identifier
application number: M017
HAN-I-SIZEHAN-I-SIZEMomar, Inc.05e1f56d-2ee9-d13f-e063-6294a90afc912023-12-11WarningsExact identifier
unii: 3K9958V90M
Rite Aid Extra Strength Itch StoppingDIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATERite Aid0c4170dd-e1fa-d549-e063-6394a90a5c232023-12-11WarningsExact identifier
application number: M017
Westlake Itch ReliefDIPHENHYDRAMINE HCL, ZINC ACETATEWestlake HB Pharma LLC0c416ba6-b01f-0609-e063-6294a90ae2a12023-12-11WarningsExact identifier
application number: M017
CVS Regular Strength Itch StoppingDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATECVS87473ace-d834-e43f-e053-2a95a90a819c2023-12-11WarningsExact identifier
application number: M017
INSTANTINSTANTUltra-Chem, Inc.0c425c6e-6c05-1748-e063-6394a90a9b5e2023-12-11WarningsExact identifier
unii: 3K9958V90M
AntiochPharma Hand SanitizerALCOHOLWeeks & Leoa1a0d368-b004-59b8-e053-2995a90ab4b12023-12-11WarningsExact identifier
unii: 3K9958V90M
La Roche Posay Laboratoire Dermatologique Cicaplast Defense B5 Skin ProtectantGLYCERINL'Oreal USA Products Inc32eaaaab-41bd-4efe-a71d-92e3a702c1e52023-12-11WarningsExact identifier
unii: PDC6A3C0OX
La Roche Posay Laboratoire Dermatologique Cicaplast Defense B5GLYCERINCosmetique Active Production01c8a0d5-bcd1-4639-be45-530a226401f02023-12-11WarningsExact identifier
unii: PDC6A3C0OX
Algonquin HanSanALCOHOLWhisk Products, Inc.1808f5ab-4bee-4768-995b-911b10cfa18b2023-12-08WarningsExact identifier
unii: 3K9958V90M
D-GermALCOHOLWhisk Products, Inc.fe08fb0c-007c-40a7-e053-6294a90acac92023-12-08WarningsExact identifier
unii: 3K9958V90M
Pacific Breeze Instant Hand Sanitizer GelALCOHOLWhisk Products, Inc.3f574300-b05a-4f98-98fa-dd2177bb3d752023-12-08WarningsExact identifier
unii: 3K9958V90M
Pretty Pump Hand SanitizerALCOHOLWhisk Products, Inc.c6d6ca9a-9fe7-4a6d-8179-e085a4b414c82023-12-08WarningsExact identifier
unii: 3K9958V90M
Katinko External Analgesic OilCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.5881fc35-3293-4f0b-801a-afcd6feb94962023-12-08WarningsExact identifier
application number: M017
Katinko Pain And Itch RelievingCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.fe907fa4-4a01-4974-b71f-9cd980b4eaa22023-12-08Warnings, Adverse reactionsExact identifier
application number: M017
CycleMENTHOLLa Mend, Inc.cfc0bcde-ef91-1e6c-e053-2a95a90ab79e2023-12-07WarningsExact identifier
application number: M017

Reported adverse events (FAERS/openFDA)#

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