FDA.reportPublic FDA data

NDC 75568-024 - Dr. Scholls Blister Pain Relief Complete

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
75568-024
Package NDCs from labels
75568-024-01
Manufacturer
Scholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd.
Effective date
2024-12-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dr. Scholl's Blister Pain Relief Complete KitScholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd.2024-12-18HUMAN OTC DRUG LABEL
Dr. Scholl's Blister Pain Relief Complete KitScholl's Wellness Company LLC | Shanghai Sibei Cosmetic Co., Ltd.2024-12-18HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75568-024-01Dr. Scholls Blister Pain Relief Complete0.37 g in 1 PATCHPATCH2.96 g40 mg in 1g2
75568-024-01Dr. Scholls Blister Pain Relief Complete0.37 g in 1 PATCHPATCH4.44 g40 mg in 1g2
75568-024-01Dr. Scholls Blister Pain Relief Complete1 in 1 POUCHPATCH40 mg in 1g2
75568-024-01Dr. Scholls Blister Pain Relief Complete1 in 1 POUCHPATCH40 mg in 1g2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75568-024DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC]2Unmatched20250216_26e3a678-b28f-588b-e063-6394a90ac025.zip
75568-024DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC]2Unmatched20250216_d860b339-48a0-405c-a67d-f7e7a31f6351.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 22 of 307 · 6,130 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Roll Pain AwayCAPSAICINPROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA547e647b-0205-221c-e063-6294a90a757c2026-06-17WarningsExact identifier
application number: M017
Roll Pain Away LemongrassCAPSAICINPROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA547ef5c0-bc31-d83e-e063-6394a90abfa62026-06-17WarningsExact identifier
application number: M017
Roll Pain Away LavenderCAPSAICINPROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA547ef2d9-f5c7-9de1-e063-6394a90a218b2026-06-17WarningsExact identifier
application number: M017
Velloryn EXTRA STRENGTH NEUROPATHYVELLORYN EXTRA STRENGTH NEUROPATHYGUANGZHOU YUSONG FINE CHEMICLS Co., Ltd547f755f-c65c-37ef-e063-6394a90aa2202026-06-17WarningsExact identifier
application number: M017
HumalogINSULIN LISPROEli Lilly and Companyc8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f2026-06-16Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Neoteric Diabetic Skin Care 4 oz.DIMETHICONERNA PHARMA LLC536f4e79-201b-7100-e063-6394a90a4f822026-06-16WarningsExact identifier
application number: M017
Medi First Extra Strength Itch ReliefDIPHENHYDRAMINE, ZINC ACETATEUnifirst First Aid Corporation54614e5b-8c72-d308-e063-6294a90a405d2026-06-16WarningsExact identifier
application number: M017
GlowBiotics Tinted Sunscreen SPF 30ZINC OXIDERum Brands, LLC544dba29-4785-4ab6-e063-6394a90a17b32026-06-16WarningsExact identifier
unii: 15FIX9V2JP
Societe Prime and DefendZINC OXIDE SUNSCREENSociete Clinical Skincare5439bd31-5ee1-9bca-e063-6394a90a748c2026-06-16WarningsExact identifier
unii: 15FIX9V2JP
Societe CoverShield Tinted SPFZINC OXIDESociete Clinical Skincare545efbc4-82d4-f126-e063-6294a90a97102026-06-16WarningsExact identifier
unii: 15FIX9V2JP
GlycerinGLYCERIN SUPPOSITORYEverpharm LLC546347e5-841e-15ca-e063-6294a90a0c8b2026-06-16WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERIN SUPPOSITORYEverpharm LLC5463f869-2b92-4551-e063-6394a90ad6f92026-06-16WarningsExact identifier
unii: PDC6A3C0OX
Blue Ice AnalgesicMENTHOLDelon Laboratories (1990) Ltd184ed488-6e62-40c6-bb71-1d523280fd6b2026-06-16WarningsExact identifier
application number: M017
Medi-First Hydrocortisone 1 % Anti-Itch CreamHYDROCORTISONEUnifirst First Aid Corporation49f04e5d-746d-cbe9-e063-6294a90a7e882026-06-16WarningsExact identifier
application number: M017
MINICA-SGLYCERINSato Pharmaceutical Co., Ltd.687902eb-e702-4e87-a0ce-9add05e3cbc12026-06-16WarningsExact identifier
unii: PDC6A3C0OX
Lidozall ProLIDOCAINE HYDROCHLORIDEV2 Pharma LLCecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff2026-06-16WarningsExact identifier
application number: M017
Shield by HEALTHY SKIN LAB MD SUNSCREENTITANIUM DIOXIDE, ZINC OXIDEHEALTHY SKIN LAB LIMITED6838b754-9915-48ff-af35-5338dbd06ac42026-06-15WarningsExact identifier
unii: 15FIX9V2JP
Haemorrhoidal Pain ReliefANORECTAL CREAMNeilMed Pharmaceuticals Inc544a9d6f-4eaa-613e-e063-6294a90a0c502026-06-15WarningsExact identifier
unii: 98PI200987
WALGREEN GLYCERIN ADULTGLYCERIN SUPPOSITORYWalgreens20c44346-0b29-7364-e063-6294a90a648f2026-06-15WarningsExact identifier
unii: PDC6A3C0OX
WALGREENS GLYCERINGLYCERIN SUSPENSIONWalgreens20c44346-0b2b-7364-e063-6294a90a648f2026-06-15WarningsExact identifier
unii: PDC6A3C0OX

Reported adverse events (FAERS/openFDA)#

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