Vaproizing

Product NDC: 37808-397
11-digit product format: 378080397
Labeler code: 37808
Product ID: 37808-397_4b93e2d1-d129-27d5-e063-6394a90ae060
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor
Dosage form: LIQUID
Route: RESPIRATORY (INHALATION)
Labeler: H E B
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-10-06
Substance: CAMPHOR (NATURAL)
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: Vaproizing
Listing expiration: 2027-12-31

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
N20HL7Q941	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
577fda09-588a-4c2e-ada5-eeda32d1aabe	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37808-397-34	Vaproizing	1 in 1 CARTON	LIQUID	1		14
37808-397-34	Vaproizing	237 mL in 1 BOTTLE, PLASTIC	LIQUID	237		14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (NATURAL)	ACTIVE INGREDIENT	N20HL7Q941	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
CAMPHOR (NATURAL)	ACTIVE MOIETY	N20HL7Q941	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
CEDAR LEAF OIL	INACTIVE INGREDIENT	BJ169U4NLG	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
DIMETHICONE	INACTIVE INGREDIENT	92RU3N3Y1O	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
LAURETH-7	INACTIVE INGREDIENT	Z95S6G8201	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
MENTHOL	INACTIVE INGREDIENT	L7T10EIP3A	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
NUTMEG OIL	INACTIVE INGREDIENT	Z1CLM48948	VAPROIZING (CAMPHOR) LIQUID [H E B]	1
POLOXAMER 124	INACTIVE INGREDIENT	1S66E28KXA	VAPROIZING (CAMPHOR) LIQUID [H E B]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-397	VAPROIZING (CAMPHOR) LIQUID [H E B]	13	Current NDC, Legacy NDC, 2 package rows	20250503_577fda09-588a-4c2e-ada5-eeda32d1aabe.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 75 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Childrens Mucus Relief Cough Cherry Liquid	DEXTROMETHORPHAN HBR, GUAIFENSIN	Topco Associates	3170748e-b09f-4c07-9927-df43771166c5	2025-12-16	Warnings	Exact identifier application number: M012
Cold and Flu Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	QUALITY CHOICE (Chain Drug Marketing Association)	ca6d43cf-0d1f-4d3c-be7e-e3ac6a24f4fe	2025-12-16	Warnings	Exact identifier application number: M012
Cold and Flu Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	QUALITY CHOICE (Chain Drug Marketing Association)	e70d0784-53bc-4910-aade-3c9ad6e36441	2025-12-16	Warnings	Exact identifier application number: M012
Pain and Sinus	ACETAMINOPHEN AND PHENYLEPHRINE	JHK Inc dba American Safety & First Aid	88f86f5a-cc2b-4c75-b7a4-f2021922280b	2025-12-16	Warnings	Exact identifier application number: M012
Severe Congestion and Cough, Cold and Flu Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, TRIPROLIDINE HCL	Walgreen Company	b75af815-9bd4-4a7a-bc68-f42f4af50699	2025-12-16	Warnings	Exact identifier application number: M012
Cough Relief Nighttime	DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	QUALITY CHOICE (Chain Drug Marketing Association)	fe5fd29e-7f81-4633-8c3b-010d68abe701	2025-12-16	Warnings	Exact identifier application number: M012
Mucus Relief Severe Congestion and Cough Maximum Strength	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Harris Teeter, LLC	e0a62fa1-9f8a-4770-b28b-1f4f02a762e0	2025-12-16	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	Walgreen Company	8c4b59b8-dfab-4f4a-9966-f07b026a758a	2025-12-16	Warnings	Exact identifier application number: M012
Daytime Cold and Flu Non Drowsy	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	QUALITY CHOICE (Chain Drug Marketing Association)	df866cf6-0526-4e61-ac9b-245b57dd5df6	2025-12-16	Warnings	Exact identifier application number: M012
Severe Cold and Flu Relief Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Walgreens	c89200b6-4adb-452e-b931-07f631dad641	2025-12-16	Warnings	Exact identifier application number: M012
ONESSIP ADULT DAYTIME SEVERE COLD AND FLU	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI	MEDWISE LIFESCIENCES INC.	45fa9159-d74c-063a-e063-6294a90a3ed0	2025-12-15	Warnings	Exact identifier application number: M012
SudoGest Nasal Decongestant	PSEUDOEPHEDRINE HCL	Major Pharmaceuticals	5229f4b2-a194-46f8-a0bc-4510fbe52075	2025-12-15	Warnings	Exact identifier application number: M012
Topcare Nasal	OXYMETAZOLINE HYDROCHLORIDE	Topco Associates LLC	f2b2467f-2d9b-4742-b90a-95975c3b694f	2025-12-13	Warnings	Exact identifier application number: M012
Menthol Cough Drop	MENTHOL	HEB	39178eb7-ada9-30bf-e054-00144ff88e88	2025-12-13	Warnings	Exact identifier application number: M012
SF Menthol Cough Drop	MENTHOL	HEB	3a443179-b7a6-3242-e054-00144ff8d46c	2025-12-13	Warnings	Exact identifier application number: M012
Cherry cough drop	MENTHOL	HEB	39bd0ca1-348f-0ce1-e054-00144ff88e88	2025-12-13	Warnings	Exact identifier application number: M012
Strawberry Cough Drops	MENTHOL	HEB	766236e2-3302-2232-e053-2991aa0af503	2025-12-13	Warnings	Exact identifier application number: M012
Honey Lemon Cough Drop	MENTHOL	HEB	3a30a427-6ab4-24ae-e054-00144ff88e88	2025-12-13	Warnings	Exact identifier application number: M012
Mixed Berry Sore Throat and Cough Lozenges	BENZOCAINE	HEB	3063ea93-6bc2-1d18-e054-00144ff88e88	2025-12-13	Warnings	Exact identifier application number: M012
HEB Menthol Cough Drops	MENTHOL	HEB	c197855d-15b4-38fc-e053-2a95a90a2dc7	2025-12-13	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
N20HL7Q941	CAMPHOR (NATURAL)	464-49-3	CAMPHOR (NATURAL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
701961	camphor 6.2 % Inhalation Solution	PSN	577fda09-588a-4c2e-ada5-eeda32d1aabe	14
701961	camphor 62 MG/ML Inhalation Solution	SCD	577fda09-588a-4c2e-ada5-eeda32d1aabe	14
701961	camphor 6.2 % Inhalation Solution	SY	577fda09-588a-4c2e-ada5-eeda32d1aabe	14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
37808-397-34	37808039734	1 BOTTLE, PLASTIC in 1 CARTON (37808-397-34) / 237 mL in 1 BOTTLE, PLASTIC	2010-10-06	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
HEB 397.002/397AA rev 2-AB Medicated Vaporizing Steam Liquid	H E B \| Nice-Pak Products, LLC	2026-02-24	HUMAN OTC DRUG LABEL	14