Home
>
National Drug Code (NDC)
>
Luffeel
Luffeel - 50114-0150-9 - (GALPHIMIA GLAUCA FLOWERING TOP and HISTAMINE DIHYDROCHLORIDE and LUFFA OPERCULATA FRUIT and SULFUR)
Drug Information of Luffeel
| Product NDC: | 50114-0150 |
| Proprietary Name: | Luffeel |
| Non Proprietary Name: | GALPHIMIA GLAUCA FLOWERING TOP and HISTAMINE DIHYDROCHLORIDE and LUFFA OPERCULATA FRUIT and SULFUR |
| Active Ingredient(s): | 4; 12; 4; 12 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL & nbsp; GALPHIMIA GLAUCA FLOWERING TOP and HISTAMINE DIHYDROCHLORIDE and LUFFA OPERCULATA FRUIT and SULFUR |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Luffeel
| Product NDC: | 50114-0150 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110705 |
Package Information of Luffeel
| Package NDC: | 50114-0150-9 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (50114-0150-9) > 20 mL in 1 BOTTLE, PUMP |
NDC Information of Luffeel
| NDC Code | 50114-0150-9 |
| Proprietary Name | Luffeel |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (50114-0150-9) > 20 mL in 1 BOTTLE, PUMP |
| Product NDC | 50114-0150 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GALPHIMIA GLAUCA FLOWERING TOP and HISTAMINE DIHYDROCHLORIDE and LUFFA OPERCULATA FRUIT and SULFUR |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20110705 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; SULFUR |
| Strength Number | 4; 12; 4; 12 |
| Strength Unit | [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL |
| Pharmaceutical Classes |
