Docu Liquid

Product NDC: 17856-0771
11-digit product format: 178560771
Labeler code: 17856
Product ID: 17856-0771_3b3f3045-55db-5ed5-e063-6294a90aab75
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate Sodium
Dosage form: LIQUID
Route: ORAL
Labeler: ATLANTIC BIOLOGICALS CORP.
Application: M
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1997-08-01
Substance: DOCUSATE SODIUM
Active strength: 50 mg/5mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 package	package	17856-0771	17856-0771-1	D	Discontinued by firm		2026-10-12
excluded package	package	17856-0771	17856-0771-2	D	Discontinued by firm		2026-10-12

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 · 19 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 package	package	17856-0771-2	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	17856-0771-1	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	17856-0771-2	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	17856-0771-1	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	17856-0771-2	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	17856-0771-1	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	17856-0771-2	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	17856-0771-1	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	17856-0771-2	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	17856-0771-1	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	17856-0771-2	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	17856-0771-1	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	17856-0771-2	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	17856-0771-1	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Docu Liquid
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DOCUSATE SODIUM	50 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F05Q2T2JA0	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1248119	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
f4ed0721-3be9-4108-a6c9-dbbe115249e9	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
17856-0771-1	2024-05-24	Drug Facts
17856-0771-2	2024-05-24	Drug Facts
17856-0771-1	2022-01-28	Drug Facts
17856-0771-2	2022-01-28	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
17856-0771-1	Docu Liquid	50 in 1 BOX, UNIT-DOSE	LIQUID	50	3
17856-0771-1	Docu Liquid	25 mL in 1 CUP, UNIT-DOSE	LIQUID	25	3
17856-0771-2	Docu Liquid	10 mL in 1 CUP, UNIT-DOSE	LIQUID	10	3
17856-0771-2	Docu Liquid	72 in 1 BOX, UNIT-DOSE	LIQUID	72	3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
17856-0771-2	ML - Milliliter	17856-0771	c48e96da-0bd0-41c4-8dbf-13b1c32d8db9	1	2022-09-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17856-0771	DOCU LIQUID (DOCUSATE SODIUM) LIQUID [ATLANTIC BIOLOGICALS CORP.]	2	Current NDC, Legacy NDC, 4 package rows	20240526_f4ed0721-3be9-4108-a6c9-dbbe115249e9.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 6 · 111 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
THERASTAT, CHERRY	CHERRY COUGH DROPS	HART Health	e3fdd1de-8f28-4063-a590-6c44507dead1	2025-12-23	Warnings	Exact identifier application number: M
Crystal Clean Antibacterial HandSoap	BENZALKONIUM CHLORIDE	Chemcor Chemical Corporation	308969b5-5ab2-44ef-ac70-9518a5dfbee2	2025-12-22	Warnings	Exact identifier application number: M
Foaming Antibacterial Handsoap	BENZALKONIUM CHLORIDE	Chemcor Chemical Corporation	eed9b007-0dc1-4954-891f-a7a042e763aa	2025-12-22	Warnings	Exact identifier application number: M
Antibacterial Handsoap	BENZALKONIUM CHLORIDE	Chemcor Chemical Corporation	1022be5e-d515-4a06-bf2b-65774ec29a0b	2025-12-22	Warnings	Exact identifier application number: M
Healthy Hands Foaming Hand Sanitizer	N/A	Maintex	746650b8-74b7-43f0-bdfc-62a68764f936	2025-12-22	Warnings	Exact identifier application number: M
Chemcor Chemical Foaming Hand Sanitizer	BENZALKONIUM CHLORIDE	Chemcor Chemical Corporation	5c9d90c1-0381-4237-9529-398fa51b3ab4	2025-12-22	Warnings	Exact identifier application number: M
Fresh Hands	BENZALKONIUM CHLORIDE	Maintex	e174083a-8820-4fa7-8cc2-0a2c86f27cd6	2025-12-22	Warnings	Exact identifier application number: M
Aluminum Hydroxide	ALUMINUM HYDROXIDE	ATLANTIC BIOLOGICALS CORP.	60a54d4e-89c2-4329-86bf-a288527f37b5	2025-12-15	Warnings	Exact identifier application number: M
MAX relief junior	ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	ff1f6f82-0c7c-4e3f-a2bd-3185e16fa770	2025-12-10	Warnings	Exact identifier application number: M
Health One Pain Relief Cream with Lidocaine 4%	PAIN RELIEF CREAM WITH LIDOCAINE 4%	ONE2ZEE LIMITED LIABILITY COMPANY	46a2276f-9da0-4e41-92f0-b17c302c7222	2025-12-03	Warnings	Exact identifier application number: M
Health One Deep Relieving Gel	DEEP RELIEVING GEL	ONE2ZEE LIMITED LIABILITY COMPANY	41d837f1-09e4-4ce3-8c1a-725c2147c7de	2025-12-03	Warnings	Exact identifier application number: M
Hand Sanitizer	ANTISEPTIC GEL	HART Health	87fcd27f-e4bf-4ae9-ad2e-b9b11ac554cc	2025-12-02	Warnings	Exact identifier application number: M
AB 3000	BENZALKONIUM CHLORIDE	Chemco	892c8911-9f1a-4c0c-9106-6d9a90d577a9	2025-11-06	Warnings	Exact identifier application number: M
Strike Bac Antibacterial Hand	BENZALKONIUM CHLORIDE	Genlabs Corporation	4014aa67-8016-40c5-88ec-daec9dba4f45	2025-11-06	Warnings	Exact identifier application number: M
Metro Antimicrobial Hand	BENZALKONIUM CHLORIDE	Maintex	a84d83dd-2445-4d0f-b763-2c69e8248cf9	2025-11-06	Warnings	Exact identifier application number: M
Butler Clean Hands	BENZALKONIUM CHLORIDE	Maintex	3fd526a8-d197-4a12-b51b-165e706720a7	2025-11-06	Warnings	Exact identifier application number: M
First Street Dishwashing Concentrate and Antibacterial Hand	BENZALKONIUM CHLORIDE	Amerifoods Trading Company	fc81ef1a-db55-411e-8b25-7dd59dd38eda	2025-11-06	Warnings	Exact identifier application number: M
Champion Ultra Clean	BENZALKONIUM CHLORIDE	Maintex	47426f67-af14-4b42-8ada-11b364826949	2025-11-06	Warnings	Exact identifier application number: M
Premium Protection Antibacterial Hand	BENZALKONIUM CHLORIDE	Maintex	53bd6860-dde3-4525-ba1b-50f69be09abc	2025-11-06	Warnings	Exact identifier application number: M
Hy-G-Clenz	BENZALKONIUM CHLORIDE	Micronova Manufacturing, Inc.	ce96634e-1ce8-4244-b317-8e1da249de83	2025-11-06	Warnings	Exact identifier application number: M

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F05Q2T2JA0	DOCUSATE SODIUM	577-11-7	DOCUSATE SODIUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1248119	docusate sodium 50 MG in 5 mL Oral Suspension	PSN	f4ed0721-3be9-4108-a6c9-dbbe115249e9	3
1248119	docusate sodium 10 MG/ML Oral Suspension	SCD	f4ed0721-3be9-4108-a6c9-dbbe115249e9	3
1248119	docusate sodium 100 MG per 10 ML Oral Suspension	SY	f4ed0721-3be9-4108-a6c9-dbbe115249e9	3
1248119	docusate sodium 150 MG per 15 ML Oral Suspension	SY	f4ed0721-3be9-4108-a6c9-dbbe115249e9	3
1248119	docusate sodium 50 MG per 5 ML Oral Suspension	SY	f4ed0721-3be9-4108-a6c9-dbbe115249e9	3
1248119	DOSS Sodium 10 MG/ML Oral Suspension	SY	f4ed0721-3be9-4108-a6c9-dbbe115249e9	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
17856-0771-1	17856077101	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0771-1) > 25 mL in 1 CUP, UNIT-DOSE	2020-01-31	0000-00-00	No	No	Current
17856-0771-2	17856077102	72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0771-2) > 10 mL in 1 CUP, UNIT-DOSE	2020-01-31	0000-00-00	No	No	Current