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TEETHING KIDS RELIEF
TEETHING KIDS RELIEF - 60512-9060-8 - (CHAMOMILLA, ARNICA MONTANA, BORAX, HYPERICUM PERFORATUM)
Drug Information of TEETHING KIDS RELIEF
| Product NDC: | 60512-9060 |
| Proprietary Name: | TEETHING KIDS RELIEF |
| Non Proprietary Name: | CHAMOMILLA, ARNICA MONTANA, BORAX, HYPERICUM PERFORATUM |
| Active Ingredient(s): | 5; 5; 5; 5 [hp_C]/25mL; [hp_C]/25mL; [hp_C]/25mL; [hp_C]/25mL & nbsp; CHAMOMILLA, ARNICA MONTANA, BORAX, HYPERICUM PERFORATUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TEETHING KIDS RELIEF
| Product NDC: | 60512-9060 |
| Labeler Name: | HOMEOLAB USA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20080818 |
Package Information of TEETHING KIDS RELIEF
| Package NDC: | 60512-9060-8 |
| Package Description: | 1 BOTTLE in 1 CARTON (60512-9060-8) > 25 mL in 1 BOTTLE |
NDC Information of TEETHING KIDS RELIEF
| NDC Code | 60512-9060-8 |
| Proprietary Name | TEETHING KIDS RELIEF |
| Package Description | 1 BOTTLE in 1 CARTON (60512-9060-8) > 25 mL in 1 BOTTLE |
| Product NDC | 60512-9060 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHAMOMILLA, ARNICA MONTANA, BORAX, HYPERICUM PERFORATUM |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080818 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | HOMEOLAB USA INC |
| Substance Name | ARNICA MONTANA; HYPERICUM PERFORATUM; MATRICARIA RECUTITA; SODIUM BORATE |
| Strength Number | 5; 5; 5; 5 |
| Strength Unit | [hp_C]/25mL; [hp_C]/25mL; [hp_C]/25mL; [hp_C]/25mL |
| Pharmaceutical Classes |
