59088-795 NDC - DERMALOGICA OIL CONTROL ()

Drug Information

Product NDC: 59088-795
Proprietary Name: Dermalogica Oil Control
Non Proprietary Name:
Active Ingredient(s): 200 mg/1 ACETYLCYSTEINE; 47 mg/1 CALCIUM CITRATE; 800 [iU]/1 CHOLECALCIFEROL; 1000 ug/1 FOLIC ACID; 16 mg/1 MAGNESIUM CITRATE
Administration Route(s):
Dosage Form(s):
Pharmacy Class(es): Antidote [EPC]; Antidote for Acetaminophen Overdose [EPC]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Decreased Respiratory Secretion Viscosity [PE]; Increased Coagulation Factor Activity [PE]; Increased Glutathione Concentration [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Mucolytic [EPC]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Reduction Activity [MoA]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]; Vitamin D [CS]; Vitamin D [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	PureTek Corporation
Product Type:
FDA Application Number:	part333D
Marketing Category:	OTC MONOGRAPH FINAL
Start Marketing Date:	11/17/2003
End Marketing Date:	5/26/2011

Package Information

No.	Package Code	Package Description	Billing Unit
1	59088-795-05	1 TUBE in 1 CARTON (59088-795-05) / 22 mL in 1 TUBE
2	59088-795-54	30 TABLET in 1 BOTTLE, PLASTIC (59088-795-54)	EA

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	59088-795	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Dermalogica Oil Control	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	11/17/2003	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH FINAL	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	PureTek Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	59088-795	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Folcyteine	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	9/14/2023	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	PureTek Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.

59088-795 NDC - DERMALOGICA OIL CONTROL ()

Drug Information

Labeler Information

Package Information

NDC Record

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