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FACEBLOCK
FACEBLOCK - 21839-111-50 - (Titanium Dioxide and Zinc Oxide)
Drug Information of FACEBLOCK
| Product NDC: | 21839-111 |
| Proprietary Name: | FACEBLOCK |
| Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
| Active Ingredient(s): | 3.35; 4.6 mL/50mL; mL/50mL & nbsp; Titanium Dioxide and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FACEBLOCK
| Product NDC: | 21839-111 |
| Labeler Name: | Gordon Laboratories, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20051109 |
Package Information of FACEBLOCK
| Package NDC: | 21839-111-50 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (21839-111-50) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Information of FACEBLOCK
| NDC Code | 21839-111-50 |
| Proprietary Name | FACEBLOCK |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (21839-111-50) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 21839-111 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20051109 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Gordon Laboratories, Inc |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 3.35; 4.6 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |
