| Product NDC: | 68428-729 |
| Proprietary Name: | Be gone Motion Sickness |
| Non Proprietary Name: | ANAMIRTA COCCULUS SEED - STRYCHNOS NUX-VOMICA SEED - KEROSENE |
| Active Ingredient(s): | 6; 6; 6 [hp_C]/28g; [hp_C]/28g; [hp_C]/28g & nbsp; ANAMIRTA COCCULUS SEED - STRYCHNOS NUX-VOMICA SEED - KEROSENE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68428-729 |
| Labeler Name: | Washington Homeopathic Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130228 |
| Package NDC: | 68428-729-14 |
| Package Description: | 28 g in 1 BOTTLE, PLASTIC (68428-729-14) |
| NDC Code | 68428-729-14 |
| Proprietary Name | Be gone Motion Sickness |
| Package Description | 28 g in 1 BOTTLE, PLASTIC (68428-729-14) |
| Product NDC | 68428-729 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ANAMIRTA COCCULUS SEED - STRYCHNOS NUX-VOMICA SEED - KEROSENE |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20130228 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Washington Homeopathic Products |
| Substance Name | ANAMIRTA COCCULUS SEED; KEROSENE; STRYCHNOS NUX-VOMICA SEED |
| Strength Number | 6; 6; 6 |
| Strength Unit | [hp_C]/28g; [hp_C]/28g; [hp_C]/28g |
| Pharmaceutical Classes |