FDA Application
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NDC Search Results on Active Ingredient: menthol
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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EUCALYPTUS OIL; MENTHOL; CAMPHOR (SYNTHETIC) | 58933-544-02 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
EUCALYPTUS OIL; MENTHOL; CAMPHOR (SYNTHETIC) | 58933-544-03 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
EUCALYPTUS OIL; MENTHOL; CAMPHOR (SYNTHETIC) | 58933-544-05 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
EUCALYPTUS OIL; MENTHOL; CAMPHOR (SYNTHETIC) | 58933-544-06 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
EUCALYPTUS OIL; MENTHOL; CAMPHOR (SYNTHETIC) | 58933-544-15 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
EUCALYPTUS OIL; MENTHOL; CAMPHOR (SYNTHETIC) | 58933-544-45 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
MENTHOL; CAMPHOR (SYNTHETIC); EUCALYPTUS OIL | 58933-595-50 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL | 58933-671-01 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
MENTHOL | 58980-615-40 | STRATUS PHARMACEUTICALS INC | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL | 59062-1286-1 | KAS Direct LLC dba BabyGanics | part341 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
MENTHOL; CAMPHOR (SYNTHETIC); SUMATRIPTAN SUCCINATE | 59088-083-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
MENTHOL; METHYL SALICYLATE; CAMPHOR (SYNTHETIC) | 59088-202-07 | PureTek Corporation | M017 | HUMAN OTC DRUG | OTC Monograph Drug |
CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE | 59088-203-07 | PureTek Corporation | M017 | HUMAN OTC DRUG | OTC Monograph Drug |
METHYL SALICYLATE; MENTHOL | 59088-215-05 | PureTek Corporation | part348 | HUMAN OTC DRUG | OTC monograph not final |
CAMPHOR (SYNTHETIC); MENTHOL | 59088-283-07 | PureTek Corporation | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL; LIDOCAINE HYDROCHLORIDE | 59088-308-03 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
MENTHOL; METHYL SALICYLATE | 59088-434-05 | PureTek Corporation | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL; CAMPHOR (SYNTHETIC) | 59088-488-07 | PureTek Corporation | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL; LIDOCAINE HYDROCHLORIDE ANHYDROUS | 59088-587-16 | PureTek Corporation | HUMAN OTC DRUG | unapproved drug other | |
MENTHOL | 59088-954-05 | PureTek Corporation | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL | 59088-962-05 | PureTek Corporation | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL; CAPSAICIN | 59092-002-01 | HPI Health Products Inc. | part348 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
MENTHOL; METHYL SALICYLATE | 59118-837-01 | Rexall Sundown, LLC | M017 | HUMAN OTC DRUG | OTC Monograph Drug |
ZINC OXIDE; MENTHOL | 59240-001-01 | MAGVERZ INC | part347 | HUMAN OTC DRUG | OTC monograph final |
MENTHOL | 59240-002-10 | MAGVERZ INC | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL | 59240-003-01 | MAGVERZ INC | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL | 59240-004-01 | MAGVERZ INC | part341 | HUMAN OTC DRUG | OTC monograph final |
MENTHOL | 59316-001-10 | RB Health (US) LLC | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL | 59316-001-20 | RB Health (US) LLC | part348 | HUMAN OTC DRUG | OTC monograph not final |
MENTHOL | 59316-002-10 | RB Health (US) LLC | part348 | HUMAN OTC DRUG | OTC monograph not final |
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