RUE21 Ocean Breeze Antibacterial Hand Sanitizer
- Product NDC
- 50563-139
- 11-digit product format
- 505630139
- Labeler code
- 50563
- Product ID
- 50563-139_63b40786-ea37-49fb-8d61-0d995b021d83
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- ENCHANTE ACCESSORIES INC.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-07-09
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 63 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 50563-139-01 | RUE21 Ocean Breeze Antibacterial Hand Sanitizer | 29 mL in 1 BOTTLE | LIQUID | 29 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50563-139 | RUE21 OCEAN BREEZE ANTIBACTERIAL HAND SANITIZER (ALCOHOL) LIQUID [ENCHANTE ACCESSORIES INC. ] | 1 | Legacy NDC, 1 package rows | 20130717_e58134e1-f6d3-43be-a160-d45d744e2b25.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50563-139-01 | 50563013901 | 29 mL in 1 BOTTLE | 29 ml | Historical |