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Sunblock
Sunblock - 52625-101-02 - (Titanium Dioxide)
Drug Information of Sunblock
| Product NDC: | 52625-101 |
| Proprietary Name: | Sunblock |
| Non Proprietary Name: | Titanium Dioxide |
| Active Ingredient(s): | 5; 6 g/80g; g/80g & nbsp; Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunblock
| Product NDC: | 52625-101 |
| Labeler Name: | Vienna Health and Beauty Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100701 |
Package Information of Sunblock
| Package NDC: | 52625-101-02 |
| Package Description: | 1 TUBE in 1 CARTON (52625-101-02) > 80 g in 1 TUBE (52625-101-01) |
NDC Information of Sunblock
| NDC Code | 52625-101-02 |
| Proprietary Name | Sunblock |
| Package Description | 1 TUBE in 1 CARTON (52625-101-02) > 80 g in 1 TUBE (52625-101-01) |
| Product NDC | 52625-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Vienna Health and Beauty Corporation |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 5; 6 |
| Strength Unit | g/80g; g/80g |
| Pharmaceutical Classes |
