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Bruiseguard MD
Bruiseguard MD - 64269-9910-4 - (ARNICA MONTANA)
Drug Information of Bruiseguard MD
| Product NDC: | 64269-9910 |
| Proprietary Name: | Bruiseguard MD |
| Non Proprietary Name: | ARNICA MONTANA |
| Active Ingredient(s): | & nbsp; ARNICA MONTANA |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bruiseguard MD
| Product NDC: | 64269-9910 |
| Labeler Name: | Scarguard Labs, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090301 |
Package Information of Bruiseguard MD
| Package NDC: | 64269-9910-4 |
| Package Description: | 7 BLISTER PACK in 1 BOX (64269-9910-4) > 1 KIT in 1 BLISTER PACK |
NDC Information of Bruiseguard MD
| NDC Code | 64269-9910-4 |
| Proprietary Name | Bruiseguard MD |
| Package Description | 7 BLISTER PACK in 1 BOX (64269-9910-4) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 64269-9910 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20090301 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Scarguard Labs, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
