| Product NDC: | 65753-100 |
| Proprietary Name: | CoreTex Sun X SPF 30 |
| Non Proprietary Name: | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Active Ingredient(s): | 1; 5; 7.5; 5; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL & nbsp; Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65753-100 |
| Labeler Name: | CoreTex Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130125 |
| Package NDC: | 65753-100-01 |
| Package Description: | 30 mL in 1 BOTTLE, PLASTIC (65753-100-01) |
| NDC Code | 65753-100-01 |
| Proprietary Name | CoreTex Sun X SPF 30 |
| Package Description | 30 mL in 1 BOTTLE, PLASTIC (65753-100-01) |
| Product NDC | 65753-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130125 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CoreTex Products |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 1; 5; 7.5; 5; 6 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |