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LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen - 67692-241-00 - (AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE)

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Drug Information of LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen

Product NDC: 67692-241
Proprietary Name: LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen
Non Proprietary Name: AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
Active Ingredient(s): 30; 70; 20; 27    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen

Product NDC: 67692-241
Labeler Name: LUMENE OY
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121129

Package Information of LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen

Package NDC: 67692-241-00
Package Description: 50 mL in 1 BOTTLE (67692-241-00)

NDC Information of LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen

NDC Code 67692-241-00
Proprietary Name LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen
Package Description 50 mL in 1 BOTTLE (67692-241-00)
Product NDC 67692-241
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121129
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name LUMENE OY
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Strength Number 30; 70; 20; 27
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen


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