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LBEL
LBEL - 13537-089-53 - (Octinoxate, Octisalate, and Oxybenzone)
Drug Information of LBEL
| Product NDC: | 13537-089 |
| Proprietary Name: | LBEL |
| Non Proprietary Name: | Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | .075; .04; .04 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LBEL
| Product NDC: | 13537-089 |
| Labeler Name: | Ventura International LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100815 |
Package Information of LBEL
| Package NDC: | 13537-089-53 |
| Package Description: | 1 JAR in 1 BOX (13537-089-53) > 1 mL in 1 JAR (13537-089-52) |
NDC Information of LBEL
| NDC Code | 13537-089-53 |
| Proprietary Name | LBEL |
| Package Description | 1 JAR in 1 BOX (13537-089-53) > 1 mL in 1 JAR (13537-089-52) |
| Product NDC | 13537-089 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100815 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura International LTD |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | .075; .04; .04 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
