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BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15
BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15 - 11489-066-01 - (OCTINOXATE AND AVOBENZONE)
Drug Information of BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15
| Product NDC: | 11489-066 |
| Proprietary Name: | BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15 |
| Non Proprietary Name: | OCTINOXATE AND AVOBENZONE |
| Active Ingredient(s): | 1.5; 2.25 mL/50mL; mL/50mL & nbsp; OCTINOXATE AND AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15
| Product NDC: | 11489-066 |
| Labeler Name: | BCM Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100120 |
Package Information of BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15
| Package NDC: | 11489-066-01 |
| Package Description: | 1 JAR in 1 CARTON (11489-066-01) > 50 mL in 1 JAR |
NDC Information of BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15
| NDC Code | 11489-066-01 |
| Proprietary Name | BOTANICS TRIPLE ACTION DAY MOISTURE SUNSCREEN SPF 15 |
| Package Description | 1 JAR in 1 CARTON (11489-066-01) > 50 mL in 1 JAR |
| Product NDC | 11489-066 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE AND AVOBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100120 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | BCM Ltd |
| Substance Name | AVOBENZONE; OCTINOXATE |
| Strength Number | 1.5; 2.25 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |
