Product NDC: | 50114-5423 |
Proprietary Name: | Reboost |
Non Proprietary Name: | SILVER NITRATE and EUPHORBIA RESINIFERA RESIN and CALCIUM SULFIDE and LUFFA OPERCULATA FRUIT and MERCURIC IODIDE and SUS SCROFA NASAL MUCOSA and PULSATILLA VULGARIS and SINUSITISINUM |
Active Ingredient(s): | 10; 4; 2; 8; 2; 10; 13; 8 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL & nbsp; SILVER NITRATE and EUPHORBIA RESINIFERA RESIN and CALCIUM SULFIDE and LUFFA OPERCULATA FRUIT and MERCURIC IODIDE and SUS SCROFA NASAL MUCOSA and PULSATILLA VULGARIS and SINUSITISINUM |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-5423 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130211 |
Package NDC: | 50114-5423-9 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (50114-5423-9) > 20 mL in 1 BOTTLE, PUMP |
NDC Code | 50114-5423-9 |
Proprietary Name | Reboost |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (50114-5423-9) > 20 mL in 1 BOTTLE, PUMP |
Product NDC | 50114-5423 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SILVER NITRATE and EUPHORBIA RESINIFERA RESIN and CALCIUM SULFIDE and LUFFA OPERCULATA FRUIT and MERCURIC IODIDE and SUS SCROFA NASAL MUCOSA and PULSATILLA VULGARIS and SINUSITISINUM |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20130211 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | CALCIUM SULFIDE; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; PULSATILLA VULGARIS; SILVER NITRATE; SINUSITISINUM; SUS SCROFA NASAL MUCOSA |
Strength Number | 10; 4; 2; 8; 2; 10; 13; 8 |
Strength Unit | [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL |
Pharmaceutical Classes |