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Avalon Organics Essential Lift
Avalon Organics Essential Lift - 52311-604-01 - (Sunscreen)
Drug Information of Avalon Organics Essential Lift
| Product NDC: | 52311-604 |
| Proprietary Name: | Avalon Organics Essential Lift |
| Non Proprietary Name: | Sunscreen |
| Active Ingredient(s): | 8.5 g/100g & nbsp; Sunscreen |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Avalon Organics Essential Lift
| Product NDC: | 52311-604 |
| Labeler Name: | Ironwood Clay Company, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100501 |
Package Information of Avalon Organics Essential Lift
| Package NDC: | 52311-604-01 |
| Package Description: | 57 g in 1 TUBE, WITH APPLICATOR (52311-604-01) |
NDC Information of Avalon Organics Essential Lift
| NDC Code | 52311-604-01 |
| Proprietary Name | Avalon Organics Essential Lift |
| Package Description | 57 g in 1 TUBE, WITH APPLICATOR (52311-604-01) |
| Product NDC | 52311-604 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sunscreen |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ironwood Clay Company, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 8.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
