ACTIVATED CHARCOAL

Product NDC: 51662-1200
11-digit product format: 516621200
Labeler code: 51662
Product ID: 51662-1200_9ef30198-d1e0-3fa8-e053-2995a90ae895
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ACTIVATED CHARCOAL
Dosage form: SUSPENSION
Route: ORAL
Labeler: HF Acquisition Co LLC, DBA HealthFirst
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2018-12-22
Marketing end: 0000-00-00
Substance: ACTIVATED CHARCOAL
Active strength: 208 mg/mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	51662-1200		I	Inactivated by FDA		2026-08-11
excluded package	package	51662-1200	51662-1200-1	I	Inactivated by FDA		2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	51662-1200-1	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	51662-1200-1	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	51662-1200-1	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	51662-1200-1	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	51662-1200-1	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	51662-1200-1	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	51662-1200-1	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	51662-1200-1	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	51662-1200-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51662-1200-1	2025-01-30	C162847	48780-1	9d75b9d0-f091-f424-e053-dadaa90a57ce	ACTIDOSE-AQUA 25grams ACTIVATED CHARCOAL TUBE
51662-1200-1	2020-02-07	C162847	48780-1	9d75b9d0-f091-f424-e053-dadaa90a57ce	ACTIDOSE-AQUA 25grams ACTIVATED CHARCOAL TUBE
51662-1200-1	2020-01-31	C162847	48780-1	9d75b9d0-f091-f424-e053-dadaa90a57ce	ACTIDOSE-AQUA 25grams ACTIVATED CHARCOAL TUBE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51662-1200-1	ACTIVATED CHARCOAL	129 mL in 1 TUBE	SUSPENSION	129		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51662-1200	ACTIVATED CHARCOAL SUSPENSION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]	3	Legacy NDC, 1 package rows	20200220_7da3506f-2799-434c-e053-2a91aa0adabb.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
2P3VWU3H10	ACTIVATED CHARCOAL	64365-11-3	ACTIVATED CHARCOAL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
309150	activated charcoal 208 MG/mL Oral Suspension	PSN	7da3506f-2799-434c-e053-2a91aa0adabb	3
309150	activated charcoal 208 MG/ML Oral Suspension	SCD	7da3506f-2799-434c-e053-2a91aa0adabb	3
309150	activated charcoal 15 GM per 72 ML Oral Suspension	SY	7da3506f-2799-434c-e053-2a91aa0adabb	3
309150	activated charcoal 25 GM per 120 ML Oral Suspension	SY	7da3506f-2799-434c-e053-2a91aa0adabb	3
309150	activated charcoal 50 GM per 240 ML Oral Suspension	SY	7da3506f-2799-434c-e053-2a91aa0adabb	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51662-1200-1	51662120001	129 mL in 1 TUBE (51662-1200-1)	129 ml	2018-12-22	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ACTIDOSE-AQUA 25grams ACTIVATED CHARCOAL TUBE	HF Acquisition Co LLC, DBA HealthFirst	2020-02-19	HUMAN PRESCRIPTION DRUG LABEL	3