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 105 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Medi-First Sinus Decongestant	PHENYLEPHRINE HYDROCHLORIDE	Unifirst First Aid Corporation	9654f5cd-74d7-44a2-9674-666d1e94ffa7	2025-09-08	Warnings	Exact identifier application number: M012
Otis Clapp Mygrex	ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE	Unifirst First Aid Corporation	f196f2c5-a100-42b1-bd01-0327b223838e	2025-09-08	Warnings	Exact identifier application number: M012
Medique Diphen	DIPHENHYDRAMINE HYDROCHLORIDE	Unifirst First Aid Corporation	b61ee2e0-2543-447d-9fc4-23363d46ce04	2025-09-08	Warnings	Exact identifier application number: M012
Green Guard Allergy 2 Relief	PHENYLEPHRINE HYDROCHLORIDE	Unifirst First Aid Corporation	16fddca9-a66b-41e6-9423-eaf091d3971e	2025-09-08	Warnings	Exact identifier application number: M012
Medique Medi-Phenyl	PHENYLEPHRINE HYDROCHLORIDE	Unifirst First Aid Corporation	d7d62ac1-1333-4366-884b-26537766ce38	2025-09-08	Warnings	Exact identifier application number: M012
Unishield Sinus Decongestant	PHENYLEPHRINE HCL	Unishield	b8f68d9d-2d38-414a-e053-2a95a90a15ec	2025-09-08	Warnings	Exact identifier application number: M012
McKesson Sinus Pain and Pressure Relief	ACETAMINOPHEN, PHENYLEPHRINE HCL	McKesson Medical-Surgical	e0cbb213-4f4f-4045-e053-2a95a90a2a18	2025-09-08	Warnings	Exact identifier application number: M012
Medique Medicidin D	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE	Unifirst First Aid Corporation	1f172d58-4050-424b-9743-130d8e618fe8	2025-09-08	Warnings	Exact identifier application number: M012
Medique Cold Cough Product	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL ,	Unifirst First Aid Corporation	e8059137-efba-398c-e053-2a95a90a21f2	2025-09-08	Warnings	Exact identifier application number: M012
Medique Medi-Mucus	DEXTROMETHORPHAN HBR, GUAIFENESIN	Unifirst First Aid Corporation	f3bb862a-9cb8-f644-e053-2a95a90a5f4f	2025-09-08	Warnings	Exact identifier application number: M012
Physicians Care Cough and Sore Throat	MENTHOL	Acme United Corporation	4e02223d-f34b-333e-e054-00144ff8d46c	2025-09-08	Warnings	Exact identifier application number: M012
Physicians Care Non-Drowsy Cold and Cough	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Acme United	186ec543-1f23-75d6-e063-6294a90a46b9	2025-09-08	Warnings	Exact identifier application number: M012
PhysiciansCare Sinus Non-Drowsy	PHENYLEPHRINE HCL	Acme United Corporation	a6daf3ef-f386-4de4-b38e-d0b90c9ae62b	2025-09-08	Warnings	Exact identifier application number: M012
PhysiciansCare Allergy Multi-Symptom Relief	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE	Acme United Corporation	fd101c27-6ba9-4cd3-baec-a354504c37a0	2025-09-08	Warnings	Exact identifier application number: M012
Green Guard Honey Lemon Cough Drop	MENTHOL 8.6 MG	Unifirst First Aid Corporation	8a94f090-61d6-4909-e053-2995a90aee38	2025-09-08	Warnings	Exact identifier application number: M012
Green Guard Cough Drop Relief	MENTHOL	Unifirst First Aid Corporation	0fc4cb11-8ff9-4eff-9588-c73eef4e0137	2025-09-08	Warnings	Exact identifier application number: M012
Multi-Symptom Cold Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL , GUAIFENESIN, ,	Unifirst First Aid Corporation	e6ea6faf-baff-a130-e053-2a95a90a085a	2025-09-08	Warnings	Exact identifier application number: M012
MEDIQUE Medikoff Drops	MENTHOL	Unifirst First Aid Corporation	0d6b4443-16a1-4851-bb03-d7407167551d	2025-09-08	Warnings	Exact identifier application number: M012
Medique Sugar Free Medikoff Drops	MENTHOL	Unifirst First Aid Corporation	92d13e19-4e7b-4565-970e-504abf02579a	2025-09-08	Warnings	Exact identifier application number: M012
Medique at Home Diphen	DIPHENHYDRAMINE HCL	Unifirst First Aid Corporation	b56d1966-efd7-56eb-e053-2995a90a89b5	2025-09-08	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