Home NDC 69901-522 Vicks VapoSteam
Product NDC 69901-522
11-digit product format 699010522
Labeler code 69901
Product ID 69901-522_d87250b4-5f54-4fd6-8848-4841fcf0285d
Type HUMAN OTC DRUG
Nonproprietary name Camphor (synthetic)
Dosage form LIQUID
Route RESPIRATORY (INHALATION)
Labeler Kaz USA, Inc
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 1995-02-28
Substance CAMPHOR (SYNTHETIC)
Active strength .062 g/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69901-522-08 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 69901-522-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 69901-522-08 I Inactivated by FDA bd6a592717d7…303034d00443…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 69901-522-08 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 69901-522-08 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 Vicks VapoSteam
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) .062 g/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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69901-522-08 Vicks VapoSteam 1 in 1 CARTON LIQUID 1 8 69901-522-08 Vicks VapoSteam 236 mL in 1 BOTTLE, PLASTIC LIQUID 236 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Camphor (synthetic) ACTIVE INGREDIENT 5TJD82A1ET VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 camphor (synthetic) ACTIVE MOIETY 5TJD82A1ET VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Alcohol INACTIVE INGREDIENT 3K9958V90M VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Cedar Leaf Oil INACTIVE INGREDIENT BJ169U4NLG VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Eucalyptus Oil INACTIVE INGREDIENT 2R04ONI662 VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Laureth-7 INACTIVE INGREDIENT Z95S6G8201 VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Menthol, Unspecified Form INACTIVE INGREDIENT L7T10EIP3A VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Nutmeg Oil INACTIVE INGREDIENT Z1CLM48948 VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1 Poloxamer 124 INACTIVE INGREDIENT 1S66E28KXA VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69901-522 VICKS VAPOSTEAM (CAMPHOR (SYNTHETIC)) LIQUID [KAZ USA, INC] 8 Current NDC, Legacy NDC, 2 package rows 20250116_c28da455-07ad-4053-8b9e-fc559f9a3f72.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 179 of 180 · 3,583 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mucus Relief DM MUCUS RELIEF DM TopCo Associates, LLC 71674a9b-89ed-43d1-aadb-b9311fdfbdf9 2022-06-07 Warnings Exact identifier application number: M012 Daytime Nighttime Cold and Flu Relief Combo Pack DAYTIME NIGHTTIME COLD AND FLU Allegiant Health fa7ed5db-4da7-46b4-a08d-1d79cb7a5674 2022-05-19 Warnings Exact identifier application number: M012 Mucus Relief DM Immediate Release MUCUS RELIEF DM Good Sense 26a199bf-57e5-4f36-b40c-83a1187e4870 2022-05-18 Warnings Exact identifier application number: M012 Mucus Relief DM Immediate Release MUCUS RELIEF DM Allegiant Health 731f8608-ad5b-491e-a4d4-2bb0c423fed5 2022-05-18 Warnings Exact identifier application number: M012 Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL OPMX LLC b3c229a4-c772-70fb-e053-2a95a90a72db 2022-03-11 Warnings Exact identifier application number: M012 Allergy Relief CHLORPHENIRAMINE MALEATE Good Sense f88e2654-8e97-4cf6-9c36-01aeb51a9102 2021-11-30 Warnings Exact identifier application number: M012 Cold Medicine COLD MEDICINE Allegiant Health 443fbc44-2c33-4316-ad31-dcc5a5aa8f52 2021-11-23 Warnings Exact identifier application number: M012 Decongestant PE Non Drowsy PHENYLEPHRINE HCL Allegiant Health 7a3098b4-381c-4f32-97a7-87b53fd64428 2021-06-16 Warnings Exact identifier application number: M012 Mucus Relief Immediate Release GUAIFENESIN 400MG Good Sense e7c68746-7ec0-46cf-b4a3-174fab819b5e 2021-05-05 Warnings Exact identifier application number: M012 Mucus Relief Immediate Release GUAIFENESIN 400MG TopCo Associates, LLC 7d91c6ab-d161-42b9-b353-0aa8f59619f8 2021-01-21 Warnings Exact identifier application number: M012 Daytime Cold and Flu ACETAMINOPHEN 325MG/ DEXTROMETHORPHAN HBR 10MG/ PHENYLEPHRINE HCL 5MG Allegiant Health bed5f9dc-45ea-4e90-86c6-86599b6f3861 2020-11-16 Warnings Exact identifier application number: M012 Nighttime Cold and Flu Relief ACETAMINOPHEN Allegiant Health b97126d7-847d-483e-b3d1-e2b61ab1743f 2020-11-11 Warnings Exact identifier application number: M012 Cold and Allergy PHENYLEPHRINE HCL AND CHLORPHENIRAMINE MALEATE Allegiant Health 7af63769-fa56-4f1f-a2ad-5b4c108c8e4f 2019-12-12 Warnings Exact identifier application number: M012 Mucus Relief Immediate Release GUAIFENESIN Allegiant Health 221d64a2-b8c7-435a-aae4-fb58fd38108f 2019-03-26 Warnings Exact identifier application number: M012 Sleep Tabs For Nighttime use DIPHENHYDRAMINE HCL TABLETS Allegiant Health 566e40b1-e9d7-44e4-b971-eef2b7cf0a7d 2018-12-26 Warnings Exact identifier application number: M012 Allergy CHLORPHENIRAMINE MALEATE Allegiant Health 4305ad50-d2a5-4d3e-9d92-cbf26e856a16 2018-12-26 Warnings Exact identifier application number: M012 Sleep Aid DIPHENHYDRAMINE HCL 25 MG Allegiant Health dbbc535f-515a-4d9b-b799-34e60f5230bb 2018-12-21 Warnings Exact identifier application number: M012 Allergy DIPHENHYDRAMINE HCL Allegiant Health c2823bad-540f-4662-8dcc-58e9f0d94efb 2018-11-07 Warnings Exact identifier application number: M012 Nasal Decongestant PE Maximum Strength Non-Drowsy PHENYLEPHRINE 10 MG Allegiant Health 7aef00df-816a-4ea2-a2ad-beed66dd2fe4 2018-11-07 Warnings Exact identifier application number: M012 DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE Westminster Pharmaceuticals, LLC a58bfb14-28f9-4425-a5a5-aaff4847c979 2018-03-14 Warnings Exact identifier application number: M012
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69901-522-08 69901052208 1 BOTTLE, PLASTIC in 1 CARTON (69901-522-08) / 236 mL in 1 BOTTLE, PLASTIC 1995-02-28 0000-00-00 No No Current