| Product NDC: | 52456-018 |
| Proprietary Name: | GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN |
| Non Proprietary Name: | HOMOSALATE, OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 3; 8; 2 mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52456-018 |
| Labeler Name: | Rodial, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100630 |
| Package NDC: | 52456-018-50 |
| Package Description: | 1 BOTTLE in 1 BOX (52456-018-50) > 50 mL in 1 BOTTLE |
| NDC Code | 52456-018-50 |
| Proprietary Name | GLAMTOX ACTIVE DAILY MOISTURIZING SUNSCREEN |
| Package Description | 1 BOTTLE in 1 BOX (52456-018-50) > 50 mL in 1 BOTTLE |
| Product NDC | 52456-018 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTINOXATE, OXYBENZONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rodial, Ltd. |
| Substance Name | HOMOSALATE; OCTINOXATE; OXYBENZONE |
| Strength Number | 3; 8; 2 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |