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AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE
AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE - 52105-070-01 - (AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE)
Drug Information of AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE
| Product NDC: | 52105-070 |
| Proprietary Name: | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | .048; .192; .041 g/3.2g; g/3.2g; g/3.2g & nbsp; AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE
| Product NDC: | 52105-070 |
| Labeler Name: | CHROMAVIS SPA |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100329 |
Package Information of AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE
| Package NDC: | 52105-070-01 |
| Package Description: | 3.2 g in 1 CONTAINER (52105-070-01) |
NDC Information of AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE
| NDC Code | 52105-070-01 |
| Proprietary Name | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
| Package Description | 3.2 g in 1 CONTAINER (52105-070-01) |
| Product NDC | 52105-070 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CHROMAVIS SPA |
| Substance Name | AVOBENZONE; OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .048; .192; .041 |
| Strength Unit | g/3.2g; g/3.2g; g/3.2g |
| Pharmaceutical Classes |
