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LBEL
LBEL - 13537-019-02 - (OCTINOXATE and OXYBENZONE)
Drug Information of LBEL
| Product NDC: | 13537-019 |
| Proprietary Name: | LBEL |
| Non Proprietary Name: | OCTINOXATE and OXYBENZONE |
| Active Ingredient(s): | .071; .016 g/g; g/g & nbsp; OCTINOXATE and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LBEL
| Product NDC: | 13537-019 |
| Labeler Name: | Ventura Corporation Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110810 |
Package Information of LBEL
| Package NDC: | 13537-019-02 |
| Package Description: | 12 TUBE in 1 CARTON (13537-019-02) > 4 g in 1 TUBE (13537-019-01) |
NDC Information of LBEL
| NDC Code | 13537-019-02 |
| Proprietary Name | LBEL |
| Package Description | 12 TUBE in 1 CARTON (13537-019-02) > 4 g in 1 TUBE (13537-019-01) |
| Product NDC | 13537-019 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and OXYBENZONE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110810 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ventura Corporation Ltd. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | .071; .016 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
