NDC 75568-024-01 - 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
Requested NDC: 75568-024-01
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
Label	Manufacturer	Effective date	Type
Dr. Scholl's Blister Pain Relief Complete Kit	Scholl's Wellness Company LLC \| Shanghai Sibei Cosmetic Co., Ltd.	2024-12-18	HUMAN OTC DRUG LABEL
Dr. Scholl's Blister Pain Relief Complete Kit	Scholl's Wellness Company LLC \| Shanghai Sibei Cosmetic Co., Ltd.	2024-12-18	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75568-024-01	Dr. Scholls Blister Pain Relief Complete	0.37 g in 1 PATCH	PATCH	2.96 g	40 mg in 1g	2
75568-024-01	Dr. Scholls Blister Pain Relief Complete	0.37 g in 1 PATCH	PATCH	4.44 g	40 mg in 1g	2
75568-024-01	Dr. Scholls Blister Pain Relief Complete	1 in 1 POUCH	PATCH		40 mg in 1g	2
75568-024-01	Dr. Scholls Blister Pain Relief Complete	1 in 1 POUCH	PATCH		40 mg in 1g	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75568-024	DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC]	2	Unmatched	20250216_26e3a678-b28f-588b-e063-6394a90ac025.zip
75568-024	DR. SCHOLLS BLISTER PAIN RELIEF COMPLETE (LIDOCAINE) KIT [SCHOLL'S WELLNESS COMPANY LLC]	2	Unmatched	20250216_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 221 of 301 · 6,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pramoxine Itch relief	PRAMOXINE HCL 1%	CVS	e947694c-c122-0291-e053-2995a90ac39a	2024-12-11	Warnings	Exact identifier application number: M017
Arthritis Cream	TROLAMINE SALICYLATE 10%	CVS	d1663f50-479b-4d55-e053-2995a90a223f	2024-12-11	Warnings	Exact identifier application number: M017
CVS Pain Relief	MENTHOL 4%	CVS	d1660d55-1ee0-7aa2-e053-2995a90a6579	2024-12-11	Warnings	Exact identifier application number: M017
CVS Muscle Rub	MENTHOL 10%, METHYL SALICYLATE 15%	CVS Health	c72c9a95-4226-6d69-e053-2a95a90a8e1c	2024-12-11	Warnings	Exact identifier application number: M017
BENGAY ULTRA STRENGTH NON-GREASY	CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE	Kenvue Brands LLC	0a41ec65-bd0b-4fc6-807d-74f353341cc7	2024-12-11	Warnings	Exact identifier application number: M017
ERBORIAN - BB CREME AU GINSENG CLAIR SPF 20	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	LABORATOIRES M&L	ee9ae84b-c8fc-4a87-8910-46ec8ccfe1a9	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
ERBORIAN - BB CREME AU GINSENG DORE SPF 20	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	LABORATOIRES M&L	121aa873-5ca6-426b-8ece-dcb5a9f82a03	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
ERBORIAN - CC CREME HIGH DEFINITION SPF 25	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	LABORATOIRES M&L	3421b9a3-6551-406f-af3a-b3da8a01d2b2	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
ERBORIAN CC RED CORRECT SPF 25	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	Laboratoires M&L	21530925-03b7-40bb-9836-6ee4011c4a79	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
ERBORIAN CC CREME HIGH DEFINITION SPF 25 CARAMEL	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	LABORATOIRES M&L	70a5537c-a364-4dae-8ab2-8ca0cbfd11b7	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
ERBORIAN - CC CREME HIGH DEFINITION SPF25 CLAIR	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	LABORATOIRES M&L	b55be8cb-7f21-45b0-bb8f-a60182077ca3	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
Serum X	LIDOCAINE HYDROCHLORIDE	AO Biologix, LLC	e07b6268-6400-6849-e053-2a95a90a8b3e	2024-12-11	Warnings	Exact identifier application number: M017
I Conceal Flawless Foundation Broad Spectrum SPF 30 Sunscreen Deep Honey	ZINC OXIDE AND TITANIUM DIOXIDE	Allure Labs	dc792777-d8b6-3ebc-e053-2a95a90abc3f	2024-12-11	Warnings	Exact identifier unii: 15FIX9V2JP
PlusCBD Pain Cream (Penetrating) 2oz	CAMPHOR, MENTHOL	CV Sciences, Inc.	ca39d327-6bf3-3408-e053-2a95a90af2d5	2024-12-11	Warnings	Exact identifier application number: M017
Blistex Medicated	DIMETHICONE, CAMPHOR (SYNTHETIC), MENTHOL, AND PHENOL	Blistex Inc.	e95439d3-f12b-4c1c-999a-79f2ddba4cfb	2024-12-11	Warnings	Exact identifier application number: M017
Blistex Foille Medicated First Aid	BENZOCAINE AND CHLOROXYLENOL	Blistex Inc.	e2eca808-e97b-43e0-aa51-7025cc61c7a8	2024-12-11	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	J&A Digital Inc.	ff95a536-35b3-4006-b43c-cce359e86aa9	2024-12-10	Warnings	Exact identifier application number: M017
Fendall Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	afda6fc3-7615-b0be-e053-2995a90a6208	2024-12-10	Warnings	Exact identifier unii: 059QF0KO0R
Tinted Sunscreen Cream SPF 30 4-Deep Amber	TITANIUM DIOXIDE, ZINC OXIDE	C.F.E.B. - Sisley	5599922a-b020-477c-a44c-1db42ec5756a	2024-12-10	Warnings	Exact identifier unii: 15FIX9V2JP
Tinted Sunscreen SPF 30 1-Natural	TITANIUM DIOXIDE, ZINC OXIDE	C.F.E.B. - Sisley	b3d53a10-2647-492a-a05f-b97c3f716aa8	2024-12-10	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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