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: | 65753-100-07 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (65753-100-07) |
NDC Code | 65753-100-07 |
Proprietary Name | CoreTex Sun X SPF 30 |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (65753-100-07) |
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 |