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TECHNIblock ULTRA SUNSCREEN
TECHNIblock ULTRA SUNSCREEN - 49672-100-01 - (AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE)
Drug Information of TECHNIblock ULTRA SUNSCREEN
| Product NDC: | 49672-100 |
| Proprietary Name: | TECHNIblock ULTRA SUNSCREEN |
| Non Proprietary Name: | AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE |
| Active Ingredient(s): | .6; 6.3; 3.4; 5.1 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TECHNIblock ULTRA SUNSCREEN
| Product NDC: | 49672-100 |
| Labeler Name: | The Myles Group LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100405 |
Package Information of TECHNIblock ULTRA SUNSCREEN
| Package NDC: | 49672-100-01 |
| Package Description: | 125 mL in 1 PACKAGE (49672-100-01) |
NDC Information of TECHNIblock ULTRA SUNSCREEN
| NDC Code | 49672-100-01 |
| Proprietary Name | TECHNIblock ULTRA SUNSCREEN |
| Package Description | 125 mL in 1 PACKAGE (49672-100-01) |
| Product NDC | 49672-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE,OCTINOXATE,OXYBENZONE,PADIMATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100405 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Myles Group LLC |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE; PADIMATE A |
| Strength Number | .6; 6.3; 3.4; 5.1 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
