NDC 68040-702

Alcortin

1% Iodoquinol - 2% Hydrocortisone

Alcortin is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Primus Pharmaceuticals. The primary component is Hydrocortisone; Iodoquinol.

• Product ID: 68040-702_4acf85e5-f2d5-40b0-8562-2427a2ab56be
• NDC: 68040-702
• Product Type: Human Prescription Drug
• Proprietary Name: Alcortin
• Generic Name: 1% Iodoquinol - 2% Hydrocortisone
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2003-07-25
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Primus Pharmaceuticals
• Substance Name: HYDROCORTISONE; IODOQUINOL
• Active Ingredient Strength: 2 g/100g; g/100g
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 68040-702-08

64 CARTON in 1 BOX (68040-702-08) > 10 PACKET in 1 CARTON > 2 g in 1 PACKET (68040-702-02)

• Marketing Start Date: 2003-07-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68040-702-13 [68040070213]

Alcortin GEL

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2003-07-25
• Inactivation Date: 2019-10-21

NDC 68040-702-08 [68040070208]

Alcortin GEL

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2003-07-25
• Inactivation Date: 2019-10-21

NDC 68040-702-02 [68040070202]

Alcortin GEL

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2003-07-25

Drug Details

Active Ingredients

Ingredient	Strength
HYDROCORTISONE	2 g/100g

OpenFDA Data

• SPL SET ID: 995ae132-8e37-4fda-b353-ce79ab9d0bf4
• Manufacturer:
  • Primus Pharmaceuticals
• UNII:
  • 63W7IE88K8
  • WI4X0X7BPJ
• RxNorm Concept Unique ID - RxCUI:
  • 1191414
  • 544118

Pharmacological Class

• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]