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