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REOROM
REOROM - 75909-100-11 - (TITANIUM DIOXIDE)
Drug Information of REOROM
| Product NDC: | 75909-100 |
| Proprietary Name: | REOROM |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 1.22; .65 mL/60mL; mL/60mL & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REOROM
| Product NDC: | 75909-100 |
| Labeler Name: | HANBUL COSMETICS CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100401 |
Package Information of REOROM
| Package NDC: | 75909-100-11 |
| Package Description: | 60 mL in 1 CARTON (75909-100-11) |
NDC Information of REOROM
| NDC Code | 75909-100-11 |
| Proprietary Name | REOROM |
| Package Description | 60 mL in 1 CARTON (75909-100-11) |
| Product NDC | 75909-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HANBUL COSMETICS CO., LTD. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 1.22; .65 |
| Strength Unit | mL/60mL; mL/60mL |
| Pharmaceutical Classes |
