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Neutrogena Ultra Sheer Dry Touch Sunblock
Neutrogena Ultra Sheer Dry Touch Sunblock - 10812-507-03 - (Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone)
Drug Information of Neutrogena Ultra Sheer Dry Touch Sunblock
| Product NDC: | 10812-507 |
| Proprietary Name: | Neutrogena Ultra Sheer Dry Touch Sunblock |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
| Active Ingredient(s): | 30; 100; 50; 40; 50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neutrogena Ultra Sheer Dry Touch Sunblock
| Product NDC: | 10812-507 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110602 |
Package Information of Neutrogena Ultra Sheer Dry Touch Sunblock
| Package NDC: | 10812-507-03 |
| Package Description: | 2 TUBE in 1 PACKAGE (10812-507-03) > 88 mL in 1 TUBE |
NDC Information of Neutrogena Ultra Sheer Dry Touch Sunblock
| NDC Code | 10812-507-03 |
| Proprietary Name | Neutrogena Ultra Sheer Dry Touch Sunblock |
| Package Description | 2 TUBE in 1 PACKAGE (10812-507-03) > 88 mL in 1 TUBE |
| Product NDC | 10812-507 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110602 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 100; 50; 40; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
