Vaporizing

Product NDC: 0363-0055
11-digit product format: 003630055
Labeler code: 0363
Product ID: 0363-0055_4aa4969d-b50c-8dc3-e063-6294a90a8bdb
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor
Dosage form: INHALANT
Route: RESPIRATORY (INHALATION)
Labeler: Walgreen Co.
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-06-01
Substance: CAMPHOR (SYNTHETIC)
Active strength: 62 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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: Vaporizing
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	62 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
701961	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
ef4f95c8-7650-4096-9369-ea8393781bee	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-0055-34	Vaporizing	1 in 1 CARTON	INHALANT	1		17
0363-0055-34	Vaporizing	237 mL in 1 BOTTLE, PLASTIC	INHALANT	237		17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
CEDAR LEAF OIL	INACTIVE INGREDIENT	BJ169U4NLG	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
DIMETHICONE	INACTIVE INGREDIENT	92RU3N3Y1O	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
LAURETH-7	INACTIVE INGREDIENT	Z95S6G8201	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
MENTHOL	INACTIVE INGREDIENT	L7T10EIP3A	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
NUTMEG OIL	INACTIVE INGREDIENT	Z1CLM48948	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1
POLOXAMER 124	INACTIVE INGREDIENT	1S66E28KXA	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0055	VAPORIZING (CAMPHOR) INHALANT [WALGREEN CO]	16	Current NDC, Legacy NDC, 2 package rows	20250322_ef4f95c8-7650-4096-9369-ea8393781bee.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 132 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	82813342-2be2-4731-ae90-dbd5eed667a9	2024-12-10	Warnings	Exact identifier application number: M012
MOUNTAIN HERB SUGAR FREE WITH STEVIA COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	b640a5d2-a7fe-486d-a65f-e7c993f950d6	2024-12-10	Warnings	Exact identifier application number: M012
Sugar Free Mountain Herb Cough Suppressant Throat Drops	MENTHOL	Ricola USA Inc.	c3f3c062-55e5-43c1-a016-ee47a7b388a5	2024-12-10	Warnings	Exact identifier application number: M012
RICOLA MAX THROAT CARE SWISS CHERRY	MENTHOL	Ricola USA Inc.	ee4733b5-6e5a-438a-97da-110f3ef6c809	2024-12-10	Warnings	Exact identifier application number: M012
SUGAR FREE GREEN TEA WITH ECHINACEA COUGH SUPPRESSANT THROAT DROPS	MENTHOL	Ricola USA Inc.	f62fcc38-2d43-40b3-841f-c8eea9ebd1e1	2024-12-10	Warnings	Exact identifier application number: M012
DUAL ACTION HONEY LEMON COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	8a6db093-7e52-443f-8dd6-94867606fef8	2024-12-10	Warnings	Exact identifier application number: M012
RICOLA MAX THROAT CARE COOL PEPPERMINT	MENTHOL	Ricola USA Inc.	5885343e-4a6e-44f7-87a4-d52599156197	2024-12-10	Warnings	Exact identifier application number: M012
EXTRA STRENGTH WITH NATURAL MENTHOL GLACIER MINT COUGH SUPPRESSANT	MENTHOL	Ricola USA Inc.	0baf383c-886d-47ca-8a6d-221298c79446	2024-12-10	Warnings	Exact identifier application number: M012
Tussin Multi Symptom Cold CF	DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE	Best Choice (Valu Merchandisers Company)	539b8972-2a46-468e-ad27-6672d746feb7	2024-12-10	Warnings	Exact identifier application number: M012
DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola USA Inc.	db2ab9be-507d-4768-9d00-188f751b7726	2024-12-10	Warnings	Exact identifier application number: M012
Adult Allergy Relief	CALMCO ALLERGY RELIEF	CalmCo	08288825-0f38-b6a3-e063-6394a90aa358	2024-12-07	Warnings	Exact identifier application number: M012
Original Herb Cough Drops	MENTHOL	Ricola Ag	c142663f-086e-4ab7-a758-9107d7077537	2024-12-05	Warnings	Exact identifier application number: M012
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola Ag	984c9793-163c-4b97-b244-9b471966a122	2024-12-05	Warnings	Exact identifier application number: M012
BENZEDREX	PROPYLHEXEDRINE	BF ASCHER AND CO INC	00d8c237-3eee-1d9f-e063-6394a90aeb86	2024-12-05	Warnings	Exact identifier application number: M012
Cold Multi Symptom Daytime Nighttime	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Chain Drug Marketing Association	d5cbb5b0-564c-429e-b680-fa683e796393	2024-12-05	Warnings	Exact identifier application number: M012
Cold Relief Multi-Symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	TopCare	de8a623f-7b10-4d56-a74b-3737e7716ffe	2024-12-05	Warnings	Exact identifier application number: M012
Cold Max Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	TopCo Associates LLC	9773958b-c5e5-4da7-a8e9-6b6c223a2b30	2024-12-05	Warnings	Exact identifier application number: M012
Cold Plus Head Congestion Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	TopCo Associates LLC	399e0e51-c2a7-451c-b74d-d3db140cef69	2024-12-05	Warnings	Exact identifier application number: M012
Head Congestion Plus Mucus PE	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	United Natural Foods, Inc. dba UNFI	09531edc-8dbd-451f-ae02-f922e9e8c248	2024-12-05	Warnings	Exact identifier application number: M012
DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	MENTHOL	Ricola Ag	71ca8af7-172d-40da-be1e-ff3ab5568e74	2024-12-05	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
701961	camphor 6.2 % Inhalation Solution	PSN	ef4f95c8-7650-4096-9369-ea8393781bee	17
701961	camphor 62 MG/ML Inhalation Solution	SCD	ef4f95c8-7650-4096-9369-ea8393781bee	17
701961	camphor 6.2 % Inhalation Solution	SY	ef4f95c8-7650-4096-9369-ea8393781bee	17

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0055-34	00363005534	1 BOTTLE, PLASTIC in 1 CARTON (0363-0055-34) / 237 mL in 1 BOTTLE, PLASTIC	2009-06-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Walgreens 397.002-397AA rev 2-AB Medicated Vaporizing Steam Liquid	Walgreen Co. \| Nice-Pak Products, LLC	2026-02-12	HUMAN OTC DRUG LABEL	17