AURORA
- Product NDC
- 63148-807
- 11-digit product format
- 631480807
- Labeler code
- 63148
- Product ID
- 63148-807_47867315-24b5-4647-996f-b6d8d2759d37
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- APOLLO HEALTH AND BEAUTY CARE
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-03-03
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 63148-807-21 | AURORABODY WASH CRISP WATERS | 621 mL in 1 BOTTLE, PLASTIC | LIQUID | 621 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63148-807 | AURORA BODY WASH CRISP WATERS (BENZALKONIUM CHLORIDE) LIQUID [APOLLO HEALTH AND BEAUTY CARE] | 1 | Legacy NDC, 1 package rows | 20150305_368ae4d4-c17b-4411-a6d5-6caa4f20c9a3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63148-807-21 | 63148080721 | 621 mL in 1 BOTTLE, PLASTIC | 621 ml | Historical |