NDC 52191-352-01 - Hydrocortisone Acetate, Iodoquinol

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: 52191-352
Requested NDC: 52191-352-01
Package NDCs from labels: 52191-352-01, 52191-352-30
Manufacturer: Bowyn Labs, LLC
Effective date: 2023-09-07
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Hydrocortisone Acetate, Iodoquinol - Bowyn Labs, LLC	Bowyn Labs, LLC	2023-09-07	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
52191-352-01	GM - Gram	52191-352	59aee306-8a47-484b-a32d-fe99180c404b	1	2015-07-20
52191-352-30	GM - Gram	52191-352	6e3fd621-1575-4310-948b-8f99a62df7ef	1	2015-07-20

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
HYDROCORTISONE ACETATE	ACTIVE INGREDIENT	3X7931PO74	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
IODOQUINOL	ACTIVE INGREDIENT	63W7IE88K8	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
HYDROCORTISONE	ACTIVE MOIETY	WI4X0X7BPJ	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
IODOQUINOL	ACTIVE MOIETY	63W7IE88K8	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
AMINOMETHYLPROPANOL	INACTIVE INGREDIENT	LU49E6626Q	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
CARBOMER 934	INACTIVE INGREDIENT	Z135WT9208	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
MAGNESIUM ALUMINUM SILICATE	INACTIVE INGREDIENT	6M3P64V0NC	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
PALMITOYL TRIPEPTIDE-1	INACTIVE INGREDIENT	HO4ZT5S86C	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
POLACRILIN	INACTIVE INGREDIENT	RCZ785HI7S	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
PPG-20 METHYL GLUCOSE ETHER	INACTIVE INGREDIENT	3WV1T97D3K	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	HYDROCORTISONE ACETATE, IODOQUINOL CREAM [BOWYN LABS, LLC]	2

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 178 of 178 · 3,544 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
CVS Hand Sanitizer	ALCOHOL	CVS	d0081c50-c0d2-436a-ba83-5d1982ae64b7	2015-08-17	Warnings	Exact identifier unii: 3K9958V90M
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: XF417D3PSL
Instant Hand Sanitizer	ALCOHOL	Safetec of America, Inc.	f9e30645-491b-4f54-acfd-f863ee235607	2013-08-07	Warnings	Exact identifier unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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