| Product NDC: | 76138-202 |
| Proprietary Name: | SPF 30 Sunscreen Tottle w Carabiner |
| 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: | 76138-202 |
| Labeler Name: | INNOVATION SPECIALTIES |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20081201 |
| Package NDC: | 76138-202-04 |
| Package Description: | 44 mL in 1 BOTTLE (76138-202-04) |
| NDC Code | 76138-202-04 |
| Proprietary Name | SPF 30 Sunscreen Tottle w Carabiner |
| Package Description | 44 mL in 1 BOTTLE (76138-202-04) |
| Product NDC | 76138-202 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OXYBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20081201 |
| 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 |