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
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 283 of 297 · 5,924 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stopain Clinical	MENTHOL	Troy Manufacturing, Inc.	c8d4ae28-efc4-6a00-e053-2a95a90a40bf	2023-10-25	Warnings	Exact identifier application number: M017
Cryo10 Topical Analgesic	MENTHOL	Element 26 LLC	ff1d2140-9302-918c-e053-6394a90acb9a	2023-10-25	Warnings	Exact identifier application number: M017
Stopain Clinical	MENTHOL	Troy Manufacturing, Inc.	3336cc35-e773-4705-84b5-61040604beef	2023-10-25	Warnings	Exact identifier application number: M017
CARMEX Multi-Symptom 3 in 1 COLD Sore treatment External Analgesic Skin Protectant	BENZOCAINE, WHITE PETROLATUM	Carma Laboratories, Inc.	bbf0abcd-b7d6-b5e4-e053-2995a90a5240	2023-10-25	Warnings	Exact identifier application number: M017
Carmex Classic Lip Balm Medicated	CAMPHOR (SYNTHETIC), WHITE PETROLATUM	Carma Laboratories, Inc.	bbee66b9-39ff-4e7e-e053-2995a90a43be	2023-10-25	Warnings	Exact identifier application number: M017
XtraCare Ice Cold Topical Analgesic Gel	MENTHOL	Rejoice International	d38f3099-d940-44d8-aa7f-404157c5e0e3	2023-10-24	Warnings	Exact identifier application number: M017
Family Wellness	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	Zhejiang Jingwei Pharmaceutical Co., Ltd.	fefbe351-1cd9-4a2f-a43d-51e2c4eb180b	2023-10-24	Warnings	Exact identifier application number: M017
TheraPlus Plus	MENTHOL	Zhejiang Jingwei Pharmaceutical Co., Ltd.	d4119f84-eb60-4134-b58e-de13d9601199	2023-10-24	Warnings	Exact identifier application number: M017
Family Wellness	HYDROCORTISONE	Zhejiang Jingwei Pharmaceutical Co., Ltd.	cddc9c4a-7c58-4225-921a-05d6afb49178	2023-10-24	Warnings	Exact identifier application number: M017
Family Wellness	GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, PETROLATUM	Zhejiang Jingwei Pharmaceutical Co., Ltd.	fde9cd90-d63c-4058-b46e-511fecea36ec	2023-10-24	Warnings	Exact identifier unii: PDC6A3C0OX
Artistry Skin Nutrition Multi-Defense UV Protect	ZINC OXIDE, TITANIUM DIOXIDE	Access Business Group LLC	82623c46-9ec3-4331-a2db-9b8d07fa1817	2023-10-23	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Cream LIGHT to MEDIUM 02	TITANIUM DIOXIDE	TAN ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI	28b3fdff-1986-4048-9ed5-a3d784a4014e	2023-10-23	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Cream- MEDIUM 03	TITANIUM DIOXIDE	TAN ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI	65de3c45-8ec2-4d73-8a29-6203d3b47bd7	2023-10-23	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi BB Cream- MEDIUM 03	TITANIUM DIOXIDE	TAN ALIZE KOZMETIK VE TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI	9102aa2f-0308-4985-b8a8-8e105047b61f	2023-10-23	Warnings	Exact identifier unii: 15FIX9V2JP
Artistry Exact Fit Longwearing Foundation Shade Golden L4N1	TITANIUM DIOXIDE	Amway Corp	7494fe09-40e0-4152-9974-a6e8a4d7f421	2023-10-22	Warnings	Exact identifier unii: 15FIX9V2JP
Artistry Exact Fit Longwearing Foundation Shade Soleil L3W1	TITANIUM DIOXIDE	Amway Corp	cec51b88-a6b8-4b64-b3aa-830e712a3c8a	2023-10-22	Warnings	Exact identifier unii: 15FIX9V2JP
Artistry Exact Fit Longwearing Foundation Shade Tawny L3N1	TITANIUM DIOXIDE	Amway Corp	706e1504-fad7-44fa-9030-f5b948e3e79b	2023-10-22	Warnings	Exact identifier unii: 15FIX9V2JP
Artistry Exact Fit Longwearing Foundation Shade Cappuccino L5W1	TITANIUM DIOXIDE	Amway Corp	b785af89-1134-4fc6-8388-c47c52d153e0	2023-10-22	Warnings	Exact identifier unii: 15FIX9V2JP
Artistry Exact Fit Longwearing Foundation Shade Natural L2N2	TITANIUM DIOXIDE	Amway Corp	db24e10a-6957-4ce7-8b03-572caacc647a	2023-10-22	Warnings	Exact identifier unii: 15FIX9V2JP
Artistry Exact Fit Longwearing Foundation Shade Caramel L5N1	TITANIUM DIOXIDE	Amway Corp	e7d8616d-3e79-4b5e-b05b-fbb506c0203d	2023-10-22	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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