Clorox Hand Sanitizer
- Product NDC
- 69540-0025
- Requested package NDC
- 69540-0025-2
- 11-digit product format
- 695400025
- Labeler code
- 69540
- Product ID
- 69540-0025_2f6a3062-891e-971d-e063-6394a90a8536
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Brand Buzz LLC
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-19
- Substance
- ALCOHOL
- Active strength
- 71 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 69540-0025 | 69540-0025-2 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 302b2466d912… | e7b80fea0513… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 69540-0025 | 69540-0025-2 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 69540-0025 | 69540-0025-2 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… |
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
- Clorox Hand Sanitizer
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALCOHOL | 71 mL/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3K9958V90M | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2282911 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| bdd47d2f-5332-1430-e053-2a95a90a1c33 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 69540-0025-1 | 2025-03-03 | Clorox Hand Sanitizer |
| 69540-0025-2 | 2025-03-03 | Clorox Hand Sanitizer |
| 69540-0025-3 | 2025-03-03 | Clorox Hand Sanitizer |
| 69540-0025-4 | 2025-03-03 | Clorox Hand Sanitizer |
| 69540-0025-1 | 2025-01-30 | Clorox Hand Sanitizer |
| 69540-0025-2 | 2025-01-30 | Clorox Hand Sanitizer |
| 69540-0025-3 | 2025-01-30 | Clorox Hand Sanitizer |
| 69540-0025-4 | 2025-01-30 | Clorox Hand Sanitizer |
| 69540-0025-1 | 2023-02-09 | Clorox Hand Sanitizer |
| 69540-0025-2 | 2023-02-09 | Clorox Hand Sanitizer |
| 69540-0025-3 | 2023-02-09 | Clorox Hand Sanitizer |
| 69540-0025-4 | 2023-02-09 | Clorox Hand Sanitizer |
| 69540-0025-1 | 2023-01-30 | Clorox Hand Sanitizer |
| 69540-0025-2 | 2023-01-30 | Clorox Hand Sanitizer |
| 69540-0025-3 | 2023-01-30 | Clorox Hand Sanitizer |
| 69540-0025-4 | 2023-01-30 | Clorox Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69540-0025-1 | Clorox Hand Sanitizer | 100 in 1 BOX | GEL | 100 | 3 | |
| 69540-0025-1 | Clorox Hand Sanitizer | 2 mL in 1 PACKET | GEL | 2 | 3 | |
| 69540-0025-2 | Clorox Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | 3 | |
| 69540-0025-3 | Clorox Hand Sanitizer | 1000 mL in 1 BOTTLE | GEL | 1000 | 3 | |
| 69540-0025-4 | Clorox Hand Sanitizer | 1000 mL in 1 BOTTLE | GEL | 1000 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69540-0025 | CLOROX HAND SANITIZER (ALCOHOL) GEL [BRAND BUZZ LLC] | 3 | Current NDC, Legacy NDC, 5 package rows | 20250305_bdd47d2f-5332-1430-e053-2a95a90a1c33.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| BZK Pads | BENZALKONIUM CHLORIDE | Dynarex Corporation | 1409c437-ff17-481d-94be-87dd6d463ba9 | 2026-01-28 | Warnings | M003 |
| Singular Wipes Unscented | ISOPROPYL ALCOHOL | SINGULAR ENTERPRISES LLC | ac2b352f-6cb2-4683-bb41-13e8ecb186bf | 2026-01-27 | Warnings | M003 |
| Singular Wipes fresh Citrus Scent | ALCOHOL | SINGULAR ENTERPRISES LLC | 867a25d2-3d2c-4dad-bbe8-84195c03a87d | 2026-01-27 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4906f079-8c9f-e3b0-e063-6294a90ad0f8 | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4912b681-e21a-1ddf-e063-6294a90aa9f4 | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491a6d77-8a84-c76d-e063-6394a90ac61f | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491b55ca-2c7a-0eb7-e063-6394a90a9cb7 | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491c4af8-c699-7128-e063-6294a90ae0f9 | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491de8ca-07e7-0aa3-e063-6394a90ae36f | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 492793db-7dc2-8313-e063-6394a90a52bf | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4928615e-d1a9-72b8-e063-6394a90aa7ed | 2026-01-26 | Warnings | M003 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4943e51a-bb8e-745a-e063-6294a90a0a3d | 2026-01-26 | Warnings | M003 |
| Hand sanitizer | HAND SANITIZER SPRAY | Beimei Biotechnology (Guangzhou) Co., Ltd. | 49455156-1072-14f5-e063-6294a90abdff | 2026-01-26 | Warnings | M003 |
| Anti-bacterial Hand Wipes | ANTI-BACTERIAL HAND WIPES | Jinhua Aidi Daily Chemical Co., Ltd. | 494b09a4-4982-13bf-e063-6394a90a486f | 2026-01-26 | Warnings | M003 |
| Homworks Alcohol Wipes Multipurpose | ETHYL ALCOHOL | Acadian Crossing Consumer Products, LLC. | c9f0c3b3-5f39-dfa6-e053-2995a90a7644 | 2026-01-26 | Warnings | M003 |
| BZK Pads | BENZALKONIUM CHLORIDE | Dynarex Corporation | 87288939-cc34-4437-94ab-dcb997d6acd5 | 2026-01-23 | Warnings | M003 |
| BZK Pads | BENZALKONIUM CHLORIDE | Dynarex Corporation | 10454042-ff2e-44ce-b2e2-436cc004897f | 2026-01-23 | Warnings | M003 |
| Everlit Survival Sting Relief Pad | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | 3a0414ea-f862-aa0f-e063-6294a90aecb7 | 2026-01-23 | Warnings | M003 |
| Medline | POVIDONE-IODINE | Medline Industries, LP | 48ebfdd6-d346-7e26-e063-6394a90af11a | 2026-01-23 | Warnings | M003 |
| EVERLIT SURVIVAL IODINE PREP PADS | POVIDONE-IODINE | EVERLIT GLOBAL INC. | 3a03fc8d-2653-9183-e063-6294a90ad76e | 2026-01-23 | Warnings | M003 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2282911 | ethanol 71 % Topical Gel | PSN | bdd47d2f-5332-1430-e053-2a95a90a1c33 | 3 |
| 2282911 | ethanol 0.71 ML/ML Topical Gel | SCD | bdd47d2f-5332-1430-e053-2a95a90a1c33 | 3 |
| 2282911 | ethanol 71 % Topical Gel | SY | bdd47d2f-5332-1430-e053-2a95a90a1c33 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69540-0025-2 | 69540002502 | 500 mL in 1 BOTTLE (69540-0025-2) | 500 ml | 2021-03-19 | 0000-00-00 | No | No | Current |