NDC 0316-0201 - Dermasorb HC Complete Kit

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: 0316-0201
Package NDCs from labels: 0316-0201-01
Manufacturer: Crown Laboratories
Effective date: 2019-09-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Hydrocortisone Lotion with Shampoo and Body Wash - Crown Laboratories	Crown Laboratories	2019-09-10	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
HYDROCORTISONE ACETATE	ACTIVE INGREDIENT	3X7931PO74	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1
HYDROCORTISONE	ACTIVE MOIETY	WI4X0X7BPJ	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1
BENZALKONIUM CHLORIDE	INACTIVE INGREDIENT	F5UM2KM3W7	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1
POLYSORBATE 20	INACTIVE INGREDIENT	7T1F30V5YH	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]	1

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 206 of 222 · 4,434 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AMP RELIEF Pain Relief Cream	MENTHOL	COASTAL FORMULAS LLC	84ea496e-ab54-4882-93ef-600f8eb33cb4	2023-11-11	Warnings	Exact identifier unii: L7T10EIP3A
AMP RELIEF Pain Relief Cream	MENTHOL	COASTAL FORMULAS LLC	39564c67-49ab-42d4-a391-792ac69180c0	2023-11-11	Warnings	Exact identifier unii: L7T10EIP3A
NERVE ACTIVE Pain Relief Cream	MENTHOL	TOP DOG DIRECT, LLC	a8b85dcb-fd3e-4340-a945-609fc741443c	2023-11-11	Warnings	Exact identifier unii: L7T10EIP3A
GeriGentle FrostyHeat Pain Relief Patch Arm and Neck	MENTHOL	Geri-Gentle Corporation	e4429f70-667e-662b-e053-2a95a90a62ba	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
GeriGentle FrostyHeat Pain Relief Patch Back	MENTHOL	Geri-Gentle Corporation	e442b8ec-a3de-65e8-e053-2995a90af3ec	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
ORCA Pain Reliever Putty with Menthol	MENTHOL	ORCA Products, LLC	188cb01a-3d0f-43d9-983e-6475c0c5b06e	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
CVS Health Isopropyl Rubbing Alcohol	ISOPROPYL ALCOHOL	CVS Health	4678074a-16f1-5480-e054-00144ff8d46c	2023-11-10	Warnings	Exact identifier unii: ND2M416302
Care One 70 Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Ahold U.S.A., Inc.	607b6917-2880-4b1c-83c6-f1297a828ecc	2023-11-10	Warnings	Exact identifier unii: ND2M416302
Topcare 70 Isopropyl Alcohol Wipes	ISOPROPYL ALCOHOL	Topco Associates LLC	bf9ee7da-69d9-47a2-8748-6b978ca3c298	2023-11-10	Warnings	Exact identifier unii: ND2M416302
SUPER WHITE STUFF Pain Relief	MENTHOL	BLUE SPRING WELLNESS, L.L.C.	9f948fb4-4275-4a1f-83f8-cd708db4a296	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
SUPER WHITE STUFF PAIN RELIEF	MENTHOL	BLUE SPRING WELLNESS, L.L.C.	b4278b70-e9a6-4d1f-bbad-257fe437b86a	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
BLUE SPRING Foot and Leg Comfort Cream with Pain Relief	MENTHOL, CAPSAICIN	BLUE SPRING WELLNESS, L.L.C.	2f9cf514-48be-49ec-b424-0b228b4b874a	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
SUPER WHITE STUFF Pain Relief	MENTHOL	BLUE SPRING WELLNESS, L.L.C.	1231ddd2-7661-45b2-ab15-32f7fdc078a8	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
SUPER WHITE Stuff Pain Relief	MENTHOL	BLUE SPRING WELLNESS, L.L.C.	7779b26b-ae3b-4639-a6b0-826c7ab37a86	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
Alo Therapeutic Massage	MENTHOL, HISTAMINE DIHYDROCHLORIDE	Theraplex Solutions	a898d2ef-5fa0-4144-8bb5-f6d5fc3ff0d4	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
SUPER BLUE STUFF Pain Relief Cream	MENTHOL	BLUE SPRING WELLNESS, L.L.C.	066a2106-2e25-4df6-9a8d-4417ba190205	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
INVIGO FLEX Pain Relief Gel	MENTHOL	WYNNPHARM INC.	909e1d8c-c517-4d6a-8682-894f042c00f8	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
ARNIMAX Penetrating Pain Relief Gel	MENTHOL	WYNNPHARM INC.	3a31f805-19c6-4036-a663-ebef9b212007	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
ALO THERAPEUTIC MASSAGE PAIN RELIEVING	MENTHOL, HISTAMINE DIHYDROCHLORIDE	Theraplex Solutions	da004500-5e48-487b-b96f-520a3094096c	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A
Osteo Bi-Flex JOINT HEALTH PAIN RELIEVING	MENTHOL, METHYL SALICYLATE	Rexall Sundown, LLC	55c55f1c-d2b3-6363-e054-00144ff88e88	2023-11-10	Warnings	Exact identifier unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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