Gillette Clear Plus Scent Boost Cool Wave
- Product NDC
- 69423-585
- 11-digit product format
- 694230585
- Labeler code
- 69423
- Product ID
- 69423-585_e2356f3e-61b3-573f-e053-2995a90a073c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Zirconium Octachlorohydrex Gly
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- M019
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-01-03
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
- Active strength
- 17 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 69423-585 | D | Discontinued by firm | 2026-10-12 | ||
| excluded package | package | 69423-585 | 69423-585-01 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 69423-585 | 69423-585-80 | D | Discontinued by firm | 2026-10-12 |
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 | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | 69423-585 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | ||
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 69423-585 | 69423-585-01 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 69423-585 | 69423-585-80 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2 | Product name | 5 | 20250304 |
| 444b3e50-f226-46ef-bfca-2e7035d140cd | Product name | 1 | 20190611 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 87711080-88eb-65c5-b2dd-bf99e700a372 | Product name | 1 | 20140508 |
| ec2149b3-5c6d-5344-f757-c86411073075 | Product name | 1 | 20140508 |
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69423-585-01 | 69423058501 | 2 CYLINDER in 1 CELLO PACK (69423-585-01) > 80 g in 1 CYLINDER | 2 cylinder | 2022-01-03 | 0000-00-00 | No | No | Current |
| 69423-585-80 | 69423058580 | 80 g in 1 CYLINDER (69423-585-80) | 80 g | 2022-01-03 | 0000-00-00 | No | No | Current |