NDC 15631-0128

CHININUM SALICYLICUM

Chininum Salicylicum

CHININUM SALICYLICUM 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 Quinine Salicylate.

Product ID15631-0128_4cf70437-612d-42d7-a1f5-1ef2e796af56
NDC15631-0128
Product TypeHuman Otc Drug
Proprietary NameCHININUM SALICYLICUM
Generic NameChininum Salicylicum
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 NameQUININE SALICYLATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0128-0

100 PELLET in 1 PACKAGE (15631-0128-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0128-2 [15631012802]

CHININUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0128-4 [15631012804]

CHININUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0128-3 [15631012803]

CHININUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0128-0 [15631012800]

CHININUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0128-5 [15631012805]

CHININUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0128-1 [15631012801]

CHININUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

Drug Details

Active Ingredients

IngredientStrength
QUININE SALICYLATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:f6464af2-0bf4-46b5-bef0-4c2ec8e6a999
Manufacturer
UNII

NDC Crossover Matching brand name "CHININUM SALICYLICUM" or generic name "Chininum Salicylicum"

NDCBrand NameGeneric Name
0220-1321Chininum salicylicumQUININE SALICYLATE
15631-0128CHININUM SALICYLICUMCHININUM SALICYLICUM
68428-309Chininum salicylicumQUININE SALICYLATE
71919-188Chininum salicylicumQUININE SALICYLATE

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