Home > National Drug Code (NDC) > Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum

Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum - 67692-470-00 - (AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE)

Alphabetical Index


Drug Information of Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum

Product NDC: 67692-470
Proprietary Name: Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum
Non Proprietary Name: AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Active Ingredient(s): 30; 60; 20; 27    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum

Product NDC: 67692-470
Labeler Name: LUMENE OY
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130411

Package Information of Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum

Package NDC: 67692-470-00
Package Description: 1 BOX in 1 PACKAGE (67692-470-00) > 50 mL in 1 BOX

NDC Information of Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum

NDC Code 67692-470-00
Proprietary Name Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum
Package Description 1 BOX in 1 PACKAGE (67692-470-00) > 50 mL in 1 BOX
Product NDC 67692-470
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130411
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name LUMENE OY
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Strength Number 30; 60; 20; 27
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Lumene Complete Rewind Recovery Day SPF 15 Sunscreen Broad Spectrum


General Information