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 94 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Maximum Strength Mucus Relief DM	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	Wal-Mart Stores,Inc.,	a748d5ab-901c-47bb-8437-997542ecebfe	2025-10-28	Warnings	Exact identifier application number: M012
Nighttime Childrens Multi Symptoms Cold and Cough Multi-Symptom Relief	CHLORPHENIRAMINE MALEATE AND DEXTROMETHORPHAN HYDROBROMIDE	WAL-MART STORES,INC.	68a68574-0fcb-4569-be57-d9aee5f62bea	2025-10-28	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief Severe Congestion and Cough	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores,Inc.,	635009a1-6154-4c62-a4be-d4f32c2cef8d	2025-10-28	Warnings	Exact identifier application number: M012
Publix Maximum Strength	OXYMETAZOLINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	cf49a06d-f095-48bf-bcd2-a410066ff9af	2025-10-28	Warnings	Exact identifier application number: M012
Publix	OXYMETAZOLINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	283e42b9-173c-4deb-9377-ff649efc177f	2025-10-28	Warnings	Exact identifier application number: M012
Publix Extra Moisturizing	OXYMETAZOLINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	eae83b75-9d5a-4100-9304-629e54ef7752	2025-10-28	Warnings	Exact identifier application number: M012
Publix	PHENYLEPHRINE HYDROCHLORIDE	PUBLIX SUPER MARKETS, INC	f10e120d-f0b7-4c51-b29b-e8cdbb1456f3	2025-10-28	Warnings	Exact identifier application number: M012
Family Care Nasal Relief	OXYMETAZOLINE HYDROCHLORIDE	United Exchange Corp	6d0f8e9e-0503-522b-e053-2a91aa0aca35	2025-10-28	Warnings	Exact identifier application number: M012
Family Care Nasal Relief	OXYMETAZOLINE HYDROCHLORIDE	United Exchange Corp	6d0eef2f-f546-d769-e053-2991aa0a8fe4	2025-10-28	Warnings	Exact identifier application number: M012
Sinus Plus Headache	ACETAMINOPHEN, PHENYLEPHRINE HCL	Kroger Company	b622b6cb-f756-439e-8684-d45ee1ea75ab	2025-10-28	Warnings	Exact identifier application number: M012
Tussin DM Cough and Chest Congestion Adult	DEXTROMETHORPHAN HBR, GUAIFENESIN	P & L Development, LLC	4af67ba7-8892-442c-b9fb-80aba9140e05	2025-10-28	Warnings	Exact identifier application number: M012
No Drip Nasal Mist Nasal Decongestant Severe Congestion	OXYMETAZOLINE HYDROCHLORIDE	Wal-Mart Stores,Inc.,	994fa270-65bb-4097-b88a-d5ce3c0e1c79	2025-10-27	Warnings	Exact identifier application number: M012
Dye Free Childrens Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	WAL-MART STORES INC.	3652ee94-b762-4100-a305-5acbec5f795a	2025-10-27	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief Cold,Flu and Sore Throat	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN ,PHENYLEPHRINE HCL	Wal-Mart Stores,Inc.,	2fd5be4f-2bb6-4241-9e0f-be7610ae2fdc	2025-10-27	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	United Natural Foods, Inc. dba UNFI	4517c7ef-156c-42b8-a2da-165e936f0837	2025-10-27	Warnings	Exact identifier application number: M012
Allergies MY CHILD NEEDS HELP WITH	DIPHENHYDRAMINE HCL	Unconditional Love	5ad293e9-0a4b-4923-8a91-f01450726828	2025-10-27	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	Cardinal Health 110, LLC. DBA Leader	933a54d3-196d-4c5d-b26f-d18b2d2ba1df	2025-10-27	Warnings	Exact identifier application number: M012
Banophen	DIPHENHYDRAMINE HCL	Major Pharmaceuticals	69b7f7ca-7a3a-4fe6-a9bb-90b0e6ad62c1	2025-10-27	Warnings	Exact identifier application number: M012
basic care daytime severe cold and flu nighttime severe cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL	Amazon.com Services LLC	4a9fd615-b7d3-452c-ac40-d9189124faaa	2025-10-24	Warnings	Exact identifier application number: M012
allergy childrens	DIPHENHYDRAMINE HYDROCHLORIDE	Meijer Distribution Inc	622b12fa-455c-4432-a9a2-698a929bbd68	2025-10-24	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