NDC 15631-0434

TEREBINTHINA

Terebinthina

TEREBINTHINA 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 Turpentine Oil.

Product ID15631-0434_56713dce-29e6-4c21-881a-e3e534e90d5b
NDC15631-0434
Product TypeHuman Otc Drug
Proprietary NameTEREBINTHINA
Generic NameTerebinthina
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameTURPENTINE OIL
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0434-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0434-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0434-2 [15631043402]

TEREBINTHINA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0434-5 [15631043405]

TEREBINTHINA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0434-1 [15631043401]

TEREBINTHINA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0434-0 [15631043400]

TEREBINTHINA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0434-4 [15631043404]

TEREBINTHINA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0434-3 [15631043403]

TEREBINTHINA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
TURPENTINE OIL2 [hp_X]/1

OpenFDA Data

SPL SET ID:7873f8cf-8c43-4a8c-bd95-86ba57c087ff
Manufacturer
UNII

NDC Crossover Matching brand name "TEREBINTHINA" or generic name "Terebinthina"

NDCBrand NameGeneric Name
0220-4957TerebinthinaTURPENTINE OIL
0220-4958TerebinthinaTURPENTINE OIL
15631-0434TEREBINTHINATEREBINTHINA
37662-1622TerebinthinaTerebinthina
37662-1623TerebinthinaTerebinthina
37662-1624TerebinthinaTerebinthina
37662-1625TerebinthinaTerebinthina
37662-1626TerebinthinaTerebinthina
37662-1627TerebinthinaTerebinthina
37662-1628TerebinthinaTerebinthina
37662-1629TerebinthinaTerebinthina
68428-668TerebinthinaTURPENTINE
71919-669TEREBINTHINATurpentine

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