BODY PRESCRIPTIONS Aloha Infused With Vitamin E ANTIBACTERIAL FOAMING HAND
- Product NDC
- 50563-410
- 11-digit product format
- 505630410
- Labeler code
- 50563
- Product ID
- 50563-410_b9446639-808a-5aa3-e053-2a95a90ae3d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOAP
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50563-410-01 | BODY PRESCRIPTIONS Aloha Infused With Vitamin E ANTIBACTERIAL FOAMING HAND | 254 mL in 1 BOTTLE | SOAP | 254 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50563-410 | BODY PRESCRIPTIONS ALOHA INFUSED WITH VITAMIN E ANTIBACTERIAL FOAMING HAND (BENZALKONIUM CHLORIDE) SOAP [ENCHANTE ACCESSORIES INC.] | 1 | Legacy NDC, 1 package rows | 20210120_dc0f299c-0fec-43de-9cf7-8fb77bc05720.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 |
|---|
| 50563-410-01 | 50563041001 | 254 mL in 1 BOTTLE (50563-410-01) | 254 ml | 2021-01-18 | 0000-00-00 | No | No | Current |