NDC 15631-0181

EUCALYPTUS GLOBULUS

Eucalyptus Globulus

EUCALYPTUS GLOBULUS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Eucalyptus Globulus Leaf.

Product ID15631-0181_a11ad69a-19ae-78e9-e053-2a95a90a8b84
NDC15631-0181
Product TypeHuman Otc Drug
Proprietary NameEUCALYPTUS GLOBULUS
Generic NameEucalyptus Globulus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameEUCALYPTUS GLOBULUS LEAF
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0181-0

100 PELLET in 1 PACKAGE (15631-0181-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0181-1 [15631018101]

EUCALYPTUS GLOBULUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0181-5 [15631018105]

EUCALYPTUS GLOBULUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0181-3 [15631018103]

EUCALYPTUS GLOBULUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0181-2 [15631018102]

EUCALYPTUS GLOBULUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0181-0 [15631018100]

EUCALYPTUS GLOBULUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0181-4 [15631018104]

EUCALYPTUS GLOBULUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

Drug Details

Active Ingredients

IngredientStrength
EUCALYPTUS GLOBULUS LEAF1 [hp_X]/1

OpenFDA Data

SPL SET ID:6321947e-c777-4faf-a511-454f4460ffb1
Manufacturer
UNII

NDC Crossover Matching brand name "EUCALYPTUS GLOBULUS" or generic name "Eucalyptus Globulus"

NDCBrand NameGeneric Name
0220-1940Eucalyptus globulusEUCALYPTUS GLOBULUS LEAF
15631-0181EUCALYPTUS GLOBULUSEUCALYPTUS GLOBULUS
37662-0681Eucalyptus GlobulusEucalyptus Globulus
37662-0682Eucalyptus GlobulusEucalyptus Globulus
37662-0683Eucalyptus GlobulusEucalyptus Globulus
37662-0684Eucalyptus GlobulusEucalyptus Globulus
37662-0685Eucalyptus GlobulusEucalyptus Globulus
37662-0686Eucalyptus GlobulusEucalyptus Globulus
37662-0687Eucalyptus GlobulusEucalyptus Globulus
60512-6669EUCALYPTUS GLOBULUSEUCALYPTUS GLOBULUS
68428-373Eucalyptus globulusEUCALYPTUS GLOBULUS LEAF
71919-275Eucalyptus globulusEUCALYPTUS GLOBULUS LEAF
22840-2404Bluegum Eucalyptus PollenEucalyptus globulus
22840-2405Bluegum Eucalyptus PollenEucalyptus globulus
22840-4444Bluegum Eucalyptus PollenEucalyptus globulus
22840-5428Bluegum Eucalyptus PollenEucalyptus globulus
71326-207ERO LONG TIME DELAYEUCALYPTUS GLOBULUS
49643-347Eucalyptus PollenEucalyptus globulus
65044-1565POLLENS - TREES, EUCALYPTUS, EUCALYPTUS GLOBULUSEucalyptus globulus
30807-3003Quit Nits Preventativeeucalyptus globulus

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