NDC 43596-0006

LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin

Ensulizole, Homosalate, Octinoxate, Oxybenzone, Titanium Dioxide

LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Ventura Corporation, Ltd. The primary component is Ensulizole; Homosalate; Octinoxate; Oxybenzone; Titanium Dioxide.

• Product ID: 43596-0006_a4002681-ce35-45e9-8d57-7e71e9b5095b
• NDC: 43596-0006
• Product Type: Human Otc Drug
• Proprietary Name: LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin
• Generic Name: Ensulizole, Homosalate, Octinoxate, Oxybenzone, Titanium Dioxide
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2012-03-28
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: Ventura Corporation, LTD
• Substance Name: ENSULIZOLE; HOMOSALATE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
• Active Ingredient Strength: 2 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 43596-0006-0

1 mL in 1 POUCH (43596-0006-0)

• Marketing Start Date: 2012-03-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43596-0006-0 [43596000600]

LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-03-28
• Inactivation Date: 2019-11-13

NDC 43596-0006-2 [43596000602]

LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-03-28
• Inactivation Date: 2019-11-13

NDC 43596-0006-1 [43596000601]

LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-03-28
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
ENSULIZOLE	1.5 mL/100mL

OpenFDA Data

• SPL SET ID: 47a47aac-a531-4c1f-b180-14cc8b0e3478
• Manufacturer:
  • Ventura Corporation, LTD
• UNII:
  • 4Y5P7MUD51
  • 15FIX9V2JP
  • 95OOS7VE0Y
  • 9YQ9DI1W42
  • V06SV4M95S

NDC Crossover Matching brand name "LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin" or generic name "Ensulizole, Homosalate, Octinoxate, Oxybenzone, Titanium Dioxide"

NDC	Brand Name	Generic Name
43596-0006	LBEL SUPREMACIE NX JOUR Replenishing Daytime Face SPF 15 Normal To Oily Skin	ENSULIZOLE, HOMOSALATE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE
43455-0006	LBEL SUPREMACIE NX JOUR Replenishing Treatment Daytime Face SPF 15 Normal To Oily Skin	ENSULIZOLE, HOMOSALATE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE