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Ultra Sensitive Faceblock SPF 25
Ultra Sensitive Faceblock SPF 25 - 21839-011-50 - (Titanium Dioxide)
Drug Information of Ultra Sensitive Faceblock SPF 25
| Product NDC: | 21839-011 |
| Proprietary Name: | Ultra Sensitive Faceblock SPF 25 |
| Non Proprietary Name: | Titanium Dioxide |
| Active Ingredient(s): | 4000 mg/50mL & nbsp; Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra Sensitive Faceblock SPF 25
| Product NDC: | 21839-011 |
| Labeler Name: | Gordon Laboratories, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
Package Information of Ultra Sensitive Faceblock SPF 25
| Package NDC: | 21839-011-50 |
| Package Description: | 1 TUBE in 1 BOX (21839-011-50) > 50 mL in 1 TUBE |
NDC Information of Ultra Sensitive Faceblock SPF 25
| NDC Code | 21839-011-50 |
| Proprietary Name | Ultra Sensitive Faceblock SPF 25 |
| Package Description | 1 TUBE in 1 BOX (21839-011-50) > 50 mL in 1 TUBE |
| Product NDC | 21839-011 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Gordon Laboratories, Inc |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 4000 |
| Strength Unit | mg/50mL |
| Pharmaceutical Classes |
