| Product NDC: | 52295-200 |
| Proprietary Name: | SPECIFIC BEAUTY DAILY HYDRATING SPF 30 |
| Non Proprietary Name: | AVOBENZONE,OCTOCRYLENE,OCTINOXATE,OXYBENZONE,OCTISALATE |
| Active Ingredient(s): | 3; 5; 5; 2.4; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE,OCTOCRYLENE,OCTINOXATE,OXYBENZONE,OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52295-200 |
| Labeler Name: | Somabella Laboratories, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110120 |
| Package NDC: | 52295-200-60 |
| Package Description: | 60 mL in 1 PACKAGE (52295-200-60) |
| NDC Code | 52295-200-60 |
| Proprietary Name | SPECIFIC BEAUTY DAILY HYDRATING SPF 30 |
| Package Description | 60 mL in 1 PACKAGE (52295-200-60) |
| Product NDC | 52295-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE,OCTOCRYLENE,OCTINOXATE,OXYBENZONE,OCTISALATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110120 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Somabella Laboratories, LLC |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 5; 5; 2.4; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |