NDC 68040-705-02 - Alcortin A

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: 68040-705
Requested NDC: 68040-705-02
Package NDCs from labels: 68040-705-02, 68040-705-13
Manufacturer: Primus Pharmaceuticals | Sonar Products, Inc
Effective date: 2009-10-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Alcortin A - Primus Pharmaceuticals \| Sonar Products, Inc	Primus Pharmaceuticals \| Sonar Products, Inc	2009-10-30	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68040-705-13	2019-10-21	C162847	48780-1	956f9ecf-df68-621f-e053-dbdaa90a74ad	ALCORTIN® A gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68040-705-02	Alcortin A	1 g in 1 PACKET	GEL	1		1
68040-705-13	Alcortin A	24 in 1 BOX	GEL	24		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68040-705	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	1	Legacy NDC, 2 package rows	20100719_3f2abee4-2841-4725-8c11-aafb35ba6bee.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68040-705-13	GM - Gram	68040-705	3285fca6-3ad8-4ee2-9ea8-993a5d8c256e	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALOE VERA LEAF	ACTIVE INGREDIENT	ZY81Z83H0X	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	1
HYDROCORTISONE ACETATE	ACTIVE INGREDIENT	3X7931PO74	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	1
Iodoquinol	ACTIVE INGREDIENT	63W7IE88K8	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	1
ALOE VERA LEAF	ACTIVE MOIETY	ZY81Z83H0X	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	1
HYDROCORTISONE	ACTIVE MOIETY	WI4X0X7BPJ	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	1
Iodoquinol	ACTIVE MOIETY	63W7IE88K8	ALCORTIN A (HYDROCORTISONE ACETATE, ALOE VERA LEAF AND IODOQUINOL) GEL [PRIMUS PHARMACEUTICALS]	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 8 of 8 · 144 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Flora Plus	ALOE, ALUMINA, ANTIMON CRUD, ARG NIT, CHELIDONIUM MAJ, GAMBOGIA, GRAPHITES, HYDRASTIS, LYCOPODIUM, SILICEA	NET Remedies	fc1ced48-bd9f-4b3f-b786-573fba072975	2021-01-21	Warnings	Exact identifier unii: ZY81Z83H0X
Day and Night Vitals	ALLIUM SAT, ALOE, ARSENICUM ALB, BERBER VULG, CALC PHOS, CEANOTHUS, CHELIDONIUM MAJ, CHOLESTERINUM, CLEMATIS ERECTA, CONDURANGO, GAMBOGIA, HAMAMELIS, KALI BROM, KALI PHOS, LYCOPODIUM, NAT CARB, PASSIFLORA, SENNA, SILICEA, SOLIDAGO, SPIGELIA ANTH, SPONGIA, VERATRUM VIR	NET Remedies	d5ddba51-5f0c-4b06-8f87-3cd6faf64b79	2021-01-19	Warnings	Exact identifier unii: ZY81Z83H0X
Hydrocortisone Acetate	HYDROCORTISONE ACETATE	Proficient Rx LP	43ed7a9a-0aaf-4987-8367-e2490d1b8448	2020-05-07	Adverse reactions	Exact identifier unii: 3X7931PO74
9cb495f1-7fac-495a-8775-c9388c8a15d3			3f2abee4-2841-4725-8c11-aafb35ba6bee	2009-10-30	Warnings, Adverse reactions	Exact identifier spl id: 9cb495f1-7fac-495a-8775-c9388c8a15d3 spl set id: 3f2abee4-2841-4725-8c11-aafb35ba6bee

Reported adverse events (FAERS/openFDA)#

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