MedPath

ACTIVATED CHARCOAL

ACTIDOSE-AQUA 25grams ACTIVATED CHARCOAL TUBE

Approved
Approval ID

7da3506f-2799-434c-e053-2a91aa0adabb

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 19, 2020

Manufacturers
FDA

HF Acquisition Co LLC, DBA HealthFirst

DUNS: 045657305

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

ACTIVATED CHARCOAL

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code51662-1200
Product Classification
G
Generic Name
ACTIVATED CHARCOAL
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 19, 2020
FDA Product Classification

INGREDIENTS (6)

ACTIVATED CHARCOALActive
Quantity: 208 mg in 1 mL
Code: 2P3VWU3H10
Classification: ACTIB
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT
SUCROSEInactive
Code: C151H8M554
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT

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