Product NDC: | 68703-049 |
Proprietary Name: | K-OK Kiddie Calmer |
Non Proprietary Name: | Aconitinum, silicea |
Active Ingredient(s): | 6; 6 [hp_C]/100mg; [hp_C]/100mg & nbsp; Aconitinum, silicea |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68703-049 |
Labeler Name: | Native Remedies, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120801 |
Package NDC: | 68703-049-20 |
Package Description: | 20000 mg in 1 BOTTLE, GLASS (68703-049-20) |
NDC Code | 68703-049-20 |
Proprietary Name | K-OK Kiddie Calmer |
Package Description | 20000 mg in 1 BOTTLE, GLASS (68703-049-20) |
Product NDC | 68703-049 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aconitinum, silicea |
Dosage Form Name | GRANULE |
Route Name | ORAL |
Start Marketing Date | 20120801 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Native Remedies, LLC |
Substance Name | ACONITUM NAPELLUS; SILICON DIOXIDE |
Strength Number | 6; 6 |
Strength Unit | [hp_C]/100mg; [hp_C]/100mg |
Pharmaceutical Classes |