DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC

Product NDC: 63667-603
11-digit product format: 636670603
Labeler code: 63667
Product ID: 63667-603_fdd9887a-22ba-4242-9c08-77f202dc6973
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: LOZENGE
Route: ORAL
Labeler: Ricola USA Inc.
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-01-01
Substance: MENTHOL
Active strength: 8.3 mg/1
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 · 9 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	63667-603-19	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	63667-603-26	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	63667-603-19	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	63667-603-26	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	63667-603-19	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	63667-603-26	`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: DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	8.3 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1424614	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
db2ab9be-507d-4768-9d00-188f751b7726	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
63667-603-19	2023-01-18	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-26	2023-01-18	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-19	2022-01-28	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-26	2022-01-28	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-19	2020-02-10	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-26	2020-02-10	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-19	2020-01-31	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC
63667-603-26	2020-01-31	DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63667-603-19	DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC	19 in 1 BAG	LOZENGE	19		4
63667-603-26	DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC	26 in 1 BAG	LOZENGE	26		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63667-603	DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC (MENTHOL) LOZENGE [RICOLA USA INC.]	4	Current NDC, Legacy NDC, 2 package rows	20241211_db2ab9be-507d-4768-9d00-188f751b7726.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 85 of 177 · 3,534 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Daytime Cold and Flu Relief	ACETAMINOHPEN, DEXTROMETHORPHAN HBR, GUAIFENESIN PHENYLEPHRINE HCL	WALGREENS CO.	bfc58cd5-9815-43af-895d-ec6cbd10937e	2025-11-26	Warnings	Exact identifier application number: M012
Walgreen Cough and Chest Congestion	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	WALGREEN COMPANY	40c038a3-91c7-4ed0-8210-65d58b82ca2b	2025-11-26	Warnings	Exact identifier application number: M012
Mucus Relief DM Maximum Strength	DEXTROMETHORPHAN HBR AND GUAIFENESIN	WALGREENS CO	724554ab-60b8-46c8-96a8-a98242604e3b	2025-11-26	Warnings	Exact identifier application number: M012
Walgreens Grape Flavor	CHILDREN COUGH AND CHEST CONGESTION	WALGREENS	795cf1af-3847-46bc-b605-64a38e57cca2	2025-11-26	Warnings	Exact identifier application number: M012
Walgreens	CHILDRENS STUFFY NOSE AND COLD	WALGREENS CO.	7ac3de2d-1d10-49ec-a2da-da46977684ad	2025-11-26	Warnings	Exact identifier application number: M012
Childrens Chest Congestion Relief	GUAIFENESIN	WALGREENS COMPANY	c1382512-e6f3-4bdf-a9e6-4f68dd5ea553	2025-11-26	Warnings	Exact identifier application number: M012
Dye Free Wal Sleep Z	DIPHENHYDRAMINE HYDROCHLORIDE	WALGREEN CO.	96948973-09e3-4c05-8982-0494ebeaac4b	2025-11-26	Warnings	Exact identifier application number: M012
WALGREEN ADULT COUGH PLUS CHEST CONGESTION DM	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	WALGREEN COMPANY	02ad9f98-07ad-4786-a1ab-169b870fec01	2025-11-26	Warnings	Exact identifier application number: M012
Walgreen Cherry	GUAIFENESIN	WALGREEN COMPANY	1f1cb4a5-1ebd-483c-bf82-16931da00e05	2025-11-26	Warnings	Exact identifier application number: M012
Walgreen Childrens COLD PLUS COUGH PLUS SORE THROAT	ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE	WALGREENS CO.	801880b2-6116-4d26-a7bf-a669eef6ad8b	2025-11-26	Warnings	Exact identifier application number: M012
Walgreen Daytimel Kids Cold Cough plus Mucus	GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE	WALGREENS CO.	452159e0-1204-460c-981f-cace4e815c6f	2025-11-26	Warnings	Exact identifier application number: M012
Multi Symptom Wal Flu Severe Cold	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	WALGREEN CO.	9c0f3f1e-25d1-4d73-9cd7-42708aa66dcb	2025-11-25	Warnings	Exact identifier application number: M012
WALGREEN Daytime Multi Symptom Flu Relief Max Strength	ACETAMINOPHEN, DEXTROMETHORPHAN HBR	WALGREENS CO.	c92a0f47-0b7c-4034-83d1-b7d2ed8022fc	2025-11-25	Warnings	Exact identifier application number: M012
Mucus Relief DM Honey and Berry Flavor	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	WALGREENS CO.	428081f5-b7eb-42da-963c-a587a44b2a79	2025-11-25	Warnings	Exact identifier application number: M012
Walgreen NightTime Cold and Flu relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDE	WALGREENS CO.	6b3766e6-d0d4-49e0-90da-fc893aef3329	2025-11-25	Warnings	Exact identifier application number: M012
Adult Allergy Relief Dye Free	DIPHENHYDRAMINE HYDROCHLORIDE	WALGREEN COMPANY	586310f3-0014-4cfc-9d86-961b3fb7aa8c	2025-11-25	Warnings	Exact identifier application number: M012
childrens Allergy Dye Free Wal Dryl	DIPHENHYDRAMINE HYDROCHLORIDE	WALGREEN CO.	4e64e040-1662-4dc9-b33f-3e119e0b3f7b	2025-11-25	Warnings	Exact identifier application number: M012
Walgreen	NASAL	WALGREENS CO	d38f8406-d7b9-472c-a472-58968bbdb993	2025-11-25	Warnings	Exact identifier application number: M012
Theraflu Flu Relief Max Strength Nighttime	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR	Haleon US Holdings LLC	780907b8-34ba-4ec8-bcdf-b2a31bd111df	2025-11-25	Warnings	Exact identifier application number: M012
Robitussin Elderberry Maximum Strength Cough plus Chest Congestion DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	Haleon US Holdings LLC	d13efbcd-1277-45d0-8389-1ba0337f7a24	2025-11-25	Warnings	Exact identifier application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1424614	menthol 8.3 MG Oral Lozenge	PSN	db2ab9be-507d-4768-9d00-188f751b7726	4
1424614	menthol 8.3 MG Oral Lozenge	SCD	db2ab9be-507d-4768-9d00-188f751b7726	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63667-603-19	63667060319	19 LOZENGE in 1 BAG (63667-603-19)	19 lozenge	2016-01-01	0000-00-00	No	No	Current
63667-603-26	63667060326	26 LOZENGE in 1 BAG (63667-603-26)	26 lozenge	2016-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DUAL ACTION GLACIER MINT SUPPRESSANT ORAL ANESTHETIC	Ricola USA Inc. \| Ricola Ag	2024-12-10	HUMAN OTC DRUG LABEL	4