PHOSPHORUS

Product NDC
15631-2887
Type
HUMAN OTC DRUG
Nonproprietary name
PHOSPHORUS
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
PHOSPHORUS
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
15631-2887-010 mL in 1 BOTTLE (15631-2887-0) 2024-05-23NoHistorical
15631-2887-130 mL in 1 BOTTLE (15631-2887-1) 2024-05-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PHOSPHORUS - Rxhomeo Private Limited d.b.a. Rxhomeo, IncRxhomeo Private Limited d.b.a. Rxhomeo, Inc2024-06-07HUMAN OTC DRUG LABEL1