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ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE
ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE - 53675-100-01 - (OCTINOXATE, OXYBENZONE)
Drug Information of ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE
| Product NDC: | 53675-100 |
| Proprietary Name: | ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 4.5 mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE
| Product NDC: | 53675-100 |
| Labeler Name: | ARUBA ALOE BALM NV |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101101 |
Package Information of ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE
| Package NDC: | 53675-100-01 |
| Package Description: | 1 JAR in 1 BOX (53675-100-01) > 118 mL in 1 JAR |
NDC Information of ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE
| NDC Code | 53675-100-01 |
| Proprietary Name | ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE |
| Package Description | 1 JAR in 1 BOX (53675-100-01) > 118 mL in 1 JAR |
| Product NDC | 53675-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ARUBA ALOE BALM NV |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 4.5 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
