Product NDC: | 76138-201 |
Proprietary Name: | SPF 30 Sunscreen Tottle |
Non Proprietary Name: | AVOBENZONE, OXYBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE |
Active Ingredient(s): | 1; 5; 7.5; 5; 3 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; AVOBENZONE, OXYBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76138-201 |
Labeler Name: | INNOVATION SPECIALTIES |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091201 |
Package NDC: | 76138-201-04 |
Package Description: | 44 mL in 1 BOTTLE (76138-201-04) |
NDC Code | 76138-201-04 |
Proprietary Name | SPF 30 Sunscreen Tottle |
Package Description | 44 mL in 1 BOTTLE (76138-201-04) |
Product NDC | 76138-201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OXYBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20091201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | INNOVATION SPECIALTIES |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 1; 5; 7.5; 5; 3 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |