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2X Sunblock SPF 50
2X Sunblock SPF 50 - 76174-120-01 - (AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OXYBENZONE)
Drug Information of 2X Sunblock SPF 50
| Product NDC: | 76174-120 |
| Proprietary Name: | 2X Sunblock SPF 50 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OXYBENZONE |
| Active Ingredient(s): | 3; 15; 6; 6 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of 2X Sunblock SPF 50
| Product NDC: | 76174-120 |
| Labeler Name: | Nupur Formulations Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110422 |
Package Information of 2X Sunblock SPF 50
| Package NDC: | 76174-120-01 |
| Package Description: | 37 mL in 1 BOTTLE (76174-120-01) |
NDC Information of 2X Sunblock SPF 50
| NDC Code | 76174-120-01 |
| Proprietary Name | 2X Sunblock SPF 50 |
| Package Description | 37 mL in 1 BOTTLE (76174-120-01) |
| Product NDC | 76174-120 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OXYBENZONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110422 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Nupur Formulations Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 15; 6; 6 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
