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I-MAX EXCELLENCE
I-MAX EXCELLENCE - 42952-101-22 - (AVOBENZONE OCTINOXATE OXYBENZONE)
Drug Information of I-MAX EXCELLENCE
| Product NDC: | 42952-101 |
| Proprietary Name: | I-MAX EXCELLENCE |
| Non Proprietary Name: | AVOBENZONE OCTINOXATE OXYBENZONE |
| Active Ingredient(s): | 2.5; 7.5; 5 g/100mL; g/100mL; g/100mL & nbsp; AVOBENZONE OCTINOXATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of I-MAX EXCELLENCE
| Product NDC: | 42952-101 |
| Labeler Name: | MAXLIFE USA, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120315 |
Package Information of I-MAX EXCELLENCE
| Package NDC: | 42952-101-22 |
| Package Description: | 59 mL in 1 BOTTLE (42952-101-22) |
NDC Information of I-MAX EXCELLENCE
| NDC Code | 42952-101-22 |
| Proprietary Name | I-MAX EXCELLENCE |
| Package Description | 59 mL in 1 BOTTLE (42952-101-22) |
| Product NDC | 42952-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE OCTINOXATE OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120315 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MAXLIFE USA, INC. |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 2.5; 7.5; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
