Product NDC: | 27293-013 |
Proprietary Name: | Baby Teething Oral Pain Reliever |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | 7.5 g/100g & nbsp; Benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 27293-013 |
Labeler Name: | Budpak Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100501 |
Package NDC: | 27293-013-01 |
Package Description: | 1 TUBE in 1 BOX (27293-013-01) > 14 g in 1 TUBE (27293-013-14) |
NDC Code | 27293-013-01 |
Proprietary Name | Baby Teething Oral Pain Reliever |
Package Description | 1 TUBE in 1 BOX (27293-013-01) > 14 g in 1 TUBE (27293-013-14) |
Product NDC | 27293-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Budpak Inc. |
Substance Name | BENZOCAINE |
Strength Number | 7.5 |
Strength Unit | g/100g |
Pharmaceutical Classes |