Geri-Tussin

Product NDC: 57896-693
11-digit product format: 578960693
Labeler code: 57896
Product ID: 57896-693_4744e526-723f-2ff0-e063-6294a90adc2b
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin
Dosage form: LIQUID
Route: ORAL
Labeler: Geri-Care Pharmaceuticals, Corp
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-05-01
Substance: GUAIFENESIN
Active strength: 100 mg/5mL
Pharmacologic classes: Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Geri-Tussin
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GUAIFENESIN	100 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
495W7451VQ	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
310604	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
65545ca3-4e93-4b59-9e17-4742e086e8e7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
4fe95224-f543-4dbb-9445-8cca122b48c8	Product name	1	20150609
e8718272-64cb-4436-969b-176c3067c8f4	Product name	1	20150609
106ff02a-57e1-4c4c-a307-fd582ff4e311	Product name	1	20150212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
57896-693-16	2021-03-15	C162847	48780-1	ba0f9c33-3e85-a910-e053-dadaa90a0b85	GeriCare- Tussin 693
57896-693-16	2021-01-29	C162847	48780-1	ba0f9c33-3e85-a910-e053-dadaa90a0b85	GeriCare- Tussin 693

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
57896-693-04	Geri-Tussin	118 mL in 1 BOTTLE	LIQUID	118	8
57896-693-08	Geri-Tussin	237 mL in 1 BOTTLE	LIQUID	237	8
57896-693-16	Geri-Tussin	473 mL in 1 BOTTLE	LIQUID	473	8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
57896-693-04	ML - Milliliter	57896-693	7f25273f-d1fc-439d-af72-925bd830bb4a	1	2024-07-12
57896-693-08	ML - Milliliter	57896-693	b5c35bb9-0318-4e23-b8fd-dff274ac9d70	1	2026-01-08
57896-693-16	ML - Milliliter	57896-693	6f03e183-fd4e-458d-b2ab-ebe17daac28b	1	2019-09-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57896-693	GERI-TUSSIN (GUAIFENESIN) LIQUID [GERI-CARE PHARMACEUTICALS, CORP]	6	Current NDC, Legacy NDC, 3 package rows	20241222_65545ca3-4e93-4b59-9e17-4742e086e8e7.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 171 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Banophen	DIPHENHYDRAMINE HCL	A-S Medication Solutions	e1b05e0c-3c61-4e2e-8e6c-ca1ed5bb93cd	2024-01-08	Warnings	Exact identifier application number: M012
AXIM DM Max	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	VIVUNT PHARMA LLC	0e7424ea-461f-5ead-e063-6294a90a41b6	2024-01-05	Warnings	Exact identifier application number: M012
AXIM Night Time - Liquid	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	VIVUNT PHARMA LLC	0e740063-80d5-c48b-e063-6394a90a3b30	2024-01-05	Warnings	Exact identifier application number: M012
AXIM DayTime - Liquid	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE	VIVUNT PHARMA LLC	0e742e10-daea-6443-e063-6294a90ab5af	2024-01-05	Warnings	Exact identifier application number: M012
Diphenhydramine HCl	DIPHENHYDRAMINE HYDROCHLORIDE	PAI Holdings, LLC dba PAI Pharma	3c3e0dc8-cddd-4f46-9b68-19bac00c07cc	2024-01-05	Warnings	Exact identifier application number: M012
Diphenhydramine HCl	DIPHENHYDRAMINE HCL	A-S Medication Solutions	fa12a5a8-bf2d-4991-9d54-9c519e8e04cd	2024-01-04	Warnings	Exact identifier application number: M012
NASAL DECONGESTANT PE 10mg	PHENYLPHRINE HCL	YYBA CORP	05824fc4-ef3f-4ebb-b601-252f76ad60ef	2024-01-03	Warnings	Exact identifier application number: M012
Diphenhydramine HCL	DIPHENHYDRAMINE HCL	Proficient Rx LP	5943d975-77e4-4cbd-b2d9-d699052fe82a	2024-01-01	Warnings	Exact identifier application number: M012
Coricidin HBP Cold and Flu	ACETAMINOPHEN AND CHLORPHENIRAMINE MALEATE	Proficient Rx LP	ac79a7dd-c26e-47d2-8fb9-768d2d09e507	2024-01-01	Warnings	Exact identifier application number: M012
Oxymethazoline HCL	OXYMETHAZOLINE HCL	Proficient Rx LP	96883e5f-18b5-4c1c-b984-756cb86be6ff	2024-01-01	Warnings	Exact identifier application number: M012
Diphenhydramine HCL	DIPHENHYDRAMINE HCL	Proficient Rx LP	6e91b9c3-57e8-488b-ac70-d863cdf9d6e8	2024-01-01	Warnings	Exact identifier application number: M012
Good Neighbor Pharmacy Childrens Allergy	DIPHENHYDRAMINE HYDROCHLORIDE	Proficient Rx LP	9e067482-8735-4476-a82e-438dd24d4289	2024-01-01	Warnings	Exact identifier application number: M012
XL-3 Day Time	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	AptaPharma Inc.	94e02be4-b8a6-422a-8f66-e6a69e924b2c	2023-12-30	Warnings	Exact identifier application number: M012
TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT DM	DEXTROMETHORPHAN HYDROBROMIDE	AptaPharma Inc.	8a4c55d0-c472-4e89-9fdb-17ecf0af4856	2023-12-30	Warnings	Exact identifier application number: M012
XL-3 Xtreme	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	AptaPharma Inc.	dff79e0b-edf0-4dd3-a722-fd9beecd6293	2023-12-30	Warnings	Exact identifier application number: M012
TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT DM	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Salado Sales, Inc.	e25727d0-7dd7-4ef5-b064-7938679f075f	2023-12-29	Warnings	Exact identifier application number: M012
Maximum Strength DM MAX	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	H E B	bb56d09d-ecb0-469e-a16f-f9f1a48942a8	2023-12-29	Warnings	Exact identifier application number: M012
Childrens Cough Mucus Relief	DEXTROMETHORPHANN HBR, GUAIFENESIN	Discount Drug Mart	2c27aca4-e1e2-419a-84c4-857718ca49da	2023-12-29	Warnings	Exact identifier application number: M012
Night Time Severe Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	Walgreen Company	de2b2e34-62a5-451f-ab68-531d1c9d4d82	2023-12-29	Warnings	Exact identifier application number: M012
H E B MAX SEVERE CONGESTION and COUGH Maxium Strength	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	H E B	d2b016ee-5329-45bf-9d71-d626204169cf	2023-12-29	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
495W7451VQ	GUAIFENESIN	93-14-1	GUAIFENESIN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
310604	guaiFENesin 100 MG in 5 mL Oral Solution	PSN	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaifenesin 20 MG/ML Oral Solution	SCD	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaifenesin 100 MG per 5 ML Oral Solution	SY	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaifenesin 100 MG per 5 ML Oral Syrup	SY	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaifenesin 200 MG per 10 ML Oral Solution	SY	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaifenesin 300 MG per 15 ML Oral Solution	SY	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaifenesin 400 MG per 20 ML Oral Solution	SY	65545ca3-4e93-4b59-9e17-4742e086e8e7	8
310604	guaiFENesin 100 MG in 5 mL Oral Solution	PSN	a307a54c-2861-4027-bec4-da8a984d211e	2
310604	guaifenesin 20 MG/ML Oral Solution	SCD	a307a54c-2861-4027-bec4-da8a984d211e	2
310604	guaifenesin 100 MG per 5 ML Oral Solution	SY	a307a54c-2861-4027-bec4-da8a984d211e	2
310604	guaifenesin 100 MG per 5 ML Oral Syrup	SY	a307a54c-2861-4027-bec4-da8a984d211e	2
310604	guaifenesin 200 MG per 10 ML Oral Solution	SY	a307a54c-2861-4027-bec4-da8a984d211e	2
310604	guaifenesin 300 MG per 15 ML Oral Solution	SY	a307a54c-2861-4027-bec4-da8a984d211e	2
310604	guaifenesin 400 MG per 20 ML Oral Solution	SY	a307a54c-2861-4027-bec4-da8a984d211e	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
57896-693-04	57896069304	118 mL in 1 BOTTLE (57896-693-04)	118 ml	2025-06-05		No	No	Current
57896-693-08	57896069308	237 mL in 1 BOTTLE (57896-693-08)	237 ml	2025-12-01		No	No	Current
57896-693-16	57896069316	473 mL in 1 BOTTLE (57896-693-16)	473 ml	2019-05-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
GeriCare- Tussin 693	Geri-Care Pharmaceuticals, Corp	2025-12-31	HUMAN OTC DRUG LABEL	8
Geri-Tussin - REMEDYREPACK INC.	REMEDYREPACK INC.	2021-03-12	HUMAN OTC DRUG LABEL	1
Geri-Tussin - ATLANTIC BIOLOGICALS CORP.	ATLANTIC BIOLOGICALS CORP.	2021-01-26	HUMAN OTC DRUG LABEL	2