Product NDC: | 37808-397 |
Proprietary Name: | Vaproizing |
Non Proprietary Name: | Camphor |
Active Ingredient(s): | 62 mg/mL & nbsp; Camphor |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37808-397 |
Labeler Name: | H E B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101006 |
Package NDC: | 37808-397-34 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37808-397-34) > 237 mL in 1 BOTTLE, PLASTIC |
NDC Code | 37808-397-34 |
Proprietary Name | Vaproizing |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37808-397-34) > 237 mL in 1 BOTTLE, PLASTIC |
Product NDC | 37808-397 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Camphor |
Dosage Form Name | LIQUID |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20101006 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H E B |
Substance Name | CAMPHOR (NATURAL) |
Strength Number | 62 |
Strength Unit | mg/mL |
Pharmaceutical Classes |