BODY PRESCRIPTIONS Aloha INFUSED WITH VITAMIN E ANTIBACTERIAL HAND
- Product NDC
- 50563-408
- 11-digit product format
- 505630408
- Labeler code
- 50563
- Product ID
- 50563-408_b94462e4-cc17-59ea-e053-2995a90aac5d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- ENCHANTE ACCESSORIES INC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-01-18
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50563-408-01 | BODY PRESCRIPTIONS Aloha INFUSED WITH VITAMIN E ANTIBACTERIAL HAND | 236.6 mL in 1 BOTTLE | LOTION | 236.6 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50563-408 | BODY PRESCRIPTIONS ALOHA INFUSED WITH VITAMIN E ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) LOTION [ENCHANTE ACCESSORIES INC.] | 1 | Legacy NDC, 1 package rows | 20210120_12668be0-eb00-41da-ae0c-0351248a6bbf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50563-408-01 | 50563040801 | 236.6 mL in 1 BOTTLE (50563-408-01) | 236.6 ml | 2021-01-18 | 0000-00-00 | No | No | Current |