| Product NDC: | 76458-201 |
| Proprietary Name: | Light Day Sunscreen Broad Spectrum SPF 37 |
| Non Proprietary Name: | Avobenzone, Octinoxate and Octocrylene |
| Active Ingredient(s): | .03; .075; .028 mL/mL; mL/mL; mL/mL & nbsp; Avobenzone, Octinoxate and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76458-201 |
| Labeler Name: | Circadia by Dr Pugliese, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120715 |
| Package NDC: | 76458-201-02 |
| Package Description: | 59 mL in 1 BOTTLE, PUMP (76458-201-02) |
| NDC Code | 76458-201-02 |
| Proprietary Name | Light Day Sunscreen Broad Spectrum SPF 37 |
| Package Description | 59 mL in 1 BOTTLE, PUMP (76458-201-02) |
| Product NDC | 76458-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120715 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Circadia by Dr Pugliese, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
| Strength Number | .03; .075; .028 |
| Strength Unit | mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |