Soft Foam Hand Sanitizer
- Product NDC
- 80891-234
- 11-digit product format
- 808910234
- Labeler code
- 80891
- Product ID
- 80891-234_d57eb1b3-06a0-43d5-e053-2a95a90a653d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Freedom Technologies LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-10-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mg/.0013mg
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 80891-234-01 | Soft Foam Hand Sanitizer | 3780 mg in 1 BOTTLE | LIQUID | 3780 | | 3 |
| 80891-234-02 | Soft Foam Hand Sanitizer | 1 in 1 BOX | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80891-234 | SOFT FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [FREEDOM TECHNOLOGIES LLC] | 3 | Legacy NDC, 2 package rows | 20220114_b2990d1f-df96-614f-e053-2a95a90a7539.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80891-234-01 | 80891023401 | 3780 mg in 1 BOTTLE | 3780 mg | | | | | Historical |
| 80891-234-02 | 80891023402 | 1 BOTTLE in 1 BOX (80891-234-02) > 3780 mg in 1 BOTTLE (80891-234-01) | 1 bottle | 2020-10-01 | 0000-00-00 | No | No | Current |