Vicks VapoSteam
- Product NDC
- 69901-522
- Requested package NDC
- 69901-522-08
- 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.
| Captured / source date | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|
| 2025-01-11 03:41 UTC · source 2025-01-10 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2022-04-09 23:13 UTC · source 2022-04-08 | I | Inactivated by FDA | 86f5da6cb304… | a595104c45d7… |
| 2022-04-04 05:40 UTC · source 2022-04-01 | I | Inactivated by FDA | bd6a592717d7… | 303034d00443… |
| 2020-06-10 20:45 UTC · source 2020-06-10 | I | Inactivated by FDA | 9bebd1f3094a… | 5416666fcb17… |
| 2019-12-08 06:16 UTC · source 2019-12-05 | 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 |
|---|---|
| CAMPHOR (SYNTHETIC) | .062 g/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5TJD82A1ET | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 701961 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c28da455-07ad-4053-8b9e-fc559f9a3f72 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2022-04-14 | Vicks ® VapoSteam ® |
| 2022-01-28 | Vicks ® VapoSteam ® |
| 2020-09-18 | Vicks ® VapoSteam ® |
| 2020-01-31 | Vicks ® VapoSteam ® |
DailyMed Package Descriptions#
| 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#
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| HISTEX-DM New Formulation | DEXTROMETHORPHAN HBR, PSEUDOEPHEDRINE HCI, AND TRIPROLIDINE HCI | Allegis Pharmaceuticals, LLC | 30010401-e5b4-2bd9-e063-6394a90a0b0b | 2025-03-10 | Warnings | M012 |
| daytime severe cold multi-symptom | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | United Natural Foods, Inc. dba UNFI | cc7c5f1c-76b7-4278-8e2a-5fbc85e022dd | 2025-03-08 | Warnings | M012 |
| Cold and Head Congestion Relief Severe | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | WinCo Foods, LLC | a39778ba-1f63-4495-8e9b-44b0bdd7f71a | 2025-03-08 | Warnings | M012 |
| Extra Strength TYLENOL Severe Cough Plus Sore Throat Day | ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE | Kenvue Brands LLC | 2e9540e4-bd1d-9370-e063-6294a90affcb | 2025-03-07 | Warnings | M012 |
| Herbal Cough Drops Original Herb | COUGH DROPS | Topco Associates LLC | 2fb22181-aee3-d0bf-e063-6294a90a7865 | 2025-03-06 | Warnings | M012 |
| REVASOL DAYTIME COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Rnv LLC | 2f9ddcc3-b913-f8b0-e063-6294a90a93ab | 2025-03-05 | Warnings | M012 |
| Herbal Throat Drops Lemon Mint Herb | THROAT DROPS | Topco Associates LLC | 2fa086b4-3b0e-0df8-e063-6294a90a6769 | 2025-03-05 | Warnings | M012 |
| Redicare Nasal and Sinus Decongestant | REDICARE NASAL AND SINUS DECONGESTANT | Redicare LLC | 2f24be68-f30e-d916-e063-6294a90a7e31 | 2025-03-04 | Warnings | M012 |
| Diphenhydramine HCl Oral Solution | DIPHENHYDRAMINE HCL ORAL SOLUTION | Kesin Pharma Corporation | 2f871005-de4d-8b2a-e063-6394a90aa43a | 2025-03-04 | Warnings | M012 |
| CVS Daytime Cough Relief Chews - Citrus Punch | DEXTROMETHORPHAN HBR | CVS | 2f885f1b-7ff5-251b-e063-6394a90a656f | 2025-03-04 | Warnings | M012 |
| CVS Dex-Dox Kids Nighttime Cough Suppressant | DEXTROMETHORPHAN HBR | CVS | 2f8b6f5e-399c-b033-e063-6294a90ac3d1 | 2025-03-04 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL 25 MG | Pioneer Life Sciences, LLC | ff8b096c-8f01-4a8c-a98f-e4aa4d688e95 | 2025-03-04 | Warnings | M012 |
| Menthol Cough Drops Honey Vanilla Flavor | MENTHOL | 7-ELEVEN | 2f3c43dd-175f-722e-e063-6294a90acff9 | 2025-02-28 | Warnings | M012 |
| Menthol Cough Drops Creamy Strawberry Flavor | MENTHOL AND PECTIN | 7-ELEVEN | 2f3c3c65-4178-6304-e063-6294a90a51fa | 2025-02-28 | Warnings | M012 |
| Menthol Cough Drops Creamy Strawberry Flavor | MENTHOL AND PECTIN | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 2efbffd7-bbdd-c5f5-e063-6294a90a15f0 | 2025-02-25 | Warnings | M012 |
| Menthol Cough Drops Honey Vanilla Flavor | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 2efc46c9-a421-1998-e063-6394a90aeb64 | 2025-02-25 | Warnings | M012 |
| Redicare Cough Drops Cherry Flavored | CHERRY FLAVORED MENTHOL COUGH DROPS | Redicare LLC | 2efeaafa-ee96-37ee-e063-6394a90a9a4b | 2025-02-25 | Warnings | M012 |
| Childrens Allergy | DIPHENHYDRAMINE HCL | Genexa Inc. | e880b8d7-61c3-41cc-e053-2995a90aaaeb | 2025-02-20 | Warnings | M012 |
| Gencare-Nasal Decongestant PE | PHENYLEPHRINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | 596ec923-56a0-4b6e-a69c-8d740feb75a2 | 2025-02-20 | Warnings | M012 |
| Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 2-pack | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Kenvue Brands LLC | 77a2dc96-73ee-4ca2-b1fe-406995802606 | 2025-02-19 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 701961 | camphor 6.2 % Inhalation Solution | PSN | c28da455-07ad-4053-8b9e-fc559f9a3f72 | 8 |
| 701961 | camphor 62 MG/ML Inhalation Solution | SCD | c28da455-07ad-4053-8b9e-fc559f9a3f72 | 8 |
| 701961 | camphor 6.2 % Inhalation Solution | SY | c28da455-07ad-4053-8b9e-fc559f9a3f72 | 8 |
Packages#
| 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 |