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 68 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MUCUS RELIEF	GUAIFENESIN 400 MG	Pioneer Life Sciences, LLC	1695e7ea-2f83-4d3a-980e-c91be6c1f2a5	2025-12-25	Warnings	Exact identifier application number: M012
GUAIFENESIN	GUAIFENESIN	Pharbest Pharmaceuticals, Inc.	0bf70fb4-d3c8-476d-b864-4eadc697a7d8	2025-12-24	Warnings	Exact identifier application number: M012
PHARBINEX-DM	GUAIFENESIN 400MG AND DEXTROMETHORPHAN HBR 20MG	Pharbest Pharmaceuticals, Inc.	8d71db43-da87-45ee-aa4a-7e870bc5016d	2025-12-24	Warnings	Exact identifier application number: M012
Daytime Nighttime Cold Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	Safeway, Inc.	764bcc58-bc5f-4ee6-82b7-cb0ed5baf3be	2025-12-23	Warnings	Exact identifier application number: M012
Tussin	GUAIFENESIN	Discount Drug Mart	14de3d6d-4eb0-42cf-8941-cb42b3dd5c71	2025-12-23	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL 25 MG	Pioneer Life Sciences, LLC	c8dcba06-a461-4af5-a120-666a63f06ac4	2025-12-23	Warnings	Exact identifier application number: M012
SAFETUSSIN MAX STRENGTH MS Cough, Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND GUAIFENESIN	KRAMER LABORATORIES	920bde5f-4079-45de-aa59-24b00e50cb56	2025-12-23	Warnings	Exact identifier application number: M012
Daytime Cold and Flu	ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE	Humanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd	46996bbf-948c-0aba-e063-6394a90a09e3	2025-12-23	Warnings	Exact identifier application number: M012
Nighttime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE	Lil' Drug Store Products, Inc.	1d2e2a5a-099b-41b3-82bd-5bf704377f78	2025-12-23	Warnings	Exact identifier application number: M012
Daytime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Lil' Drug Store Products, Inc.	5b493ed7-9044-4841-9935-236d0bdc71a9	2025-12-23	Warnings	Exact identifier application number: M012
Daytime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Lil' Drug Store Products, Inc.	77a7ff9a-a414-4053-8d8d-369907d4380d	2025-12-23	Warnings	Exact identifier application number: M012
Nighttime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE	Lil' Drug Store Products, Inc.	8f320235-f243-4211-b99c-18526e686548	2025-12-23	Warnings	Exact identifier application number: M012
Circle K Daytime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Lil' Drug Store Products, Inc.	b6a46498-d9a8-4da2-9283-57d135f305a5	2025-12-23	Warnings	Exact identifier application number: M012
Circle K Nighttime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE	Lil' Drug Store Products, Inc.	7c5faec2-28c6-4c15-a268-d8b578140b74	2025-12-23	Warnings	Exact identifier application number: M012
Sugar Free Honey Lemon Cough Drops	MENTHOL	Walmart	67650b94-adbb-87fb-e053-2a91aa0a87e6	2025-12-23	Warnings	Exact identifier application number: M012
Equate Benz-Dex Cough and Throat Lozenges	BENZOCAINE	Walmart	c0a6cb7f-a247-e610-e053-2a95a90a4199	2025-12-23	Warnings	Exact identifier application number: M012
Equate Honey Lemon Cough Drops	MENTHOL	WalMart	0028be18-5162-ff51-e063-6294a90ae517	2025-12-23	Warnings	Exact identifier application number: M012
Equate SF Menthol Cough Drops	MENTHOL	WalMart	003a229c-b014-e9f3-e063-6294a90aa5ed	2025-12-23	Warnings	Exact identifier application number: M012
Equate Menthol Cough Drops	MENTHOL	Walmart	124e6968-f59c-39d4-e063-6294a90a66d4	2025-12-23	Warnings	Exact identifier application number: M012
Equate Severe Menthol Throat Drop	MENTHOL	Walmart	125f3f5a-52aa-e398-e063-6394a90a0012	2025-12-23	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