Walgreens Hand Sanitizer Sweet Pea
- Product NDC
- 54860-532
- 11-digit product format
- 548600532
- Labeler code
- 54860
- Product ID
- 54860-532_435cacc6-70f4-63a6-e063-6394a90aab31
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- alcohol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Shenzhen Lantern Scicence Co.,Ltd.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-11
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 54860-532_435cacc6-70f4-63a6-e063-6394a90aab31
- SPL ID
- 435cacc6-70f4-63a6-e063-6394a90aab31
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- Walgreens Hand Sanitizer Sweet Pea
- Generic name
- alcohol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Marketing start
- 2025-11-11
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M003
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1041849 |
| Spl Set Id | 435ca082-0b6b-c55e-e063-6294a90af56e |
| Manufacturer Name | Shenzhen Lantern Scicence Co.,Ltd. |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 54860-532-01 | 40 mL in 1 BOTTLE, SPRAY (54860-532-01) | 2025-11-11 | Yes |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3K9958V90M | ALCOHOL | 64-17-5 | ALCOHOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 54860-532-01 | 54860053201 | 40 mL in 1 BOTTLE, SPRAY (54860-532-01) | 40 ml | 2025-11-11 | Yes | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Walgreens Hand Sanitizer Sweet Pea | Shenzhen Lantern Scicence Co.,Ltd. | Shenzhen Lantern Science Co.,Ltd. | 2025-11-11 | HUMAN OTC DRUG LABEL | 1 |