PUREHOCL
- Product NDC
- 81270-202
- 11-digit product format
- 812700202
- Labeler code
- 81270
- Product ID
- 81270-202_c1799684-8364-27c2-e053-2a95a90aa497
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PUREHOCL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- HOCL inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-05-01
- Marketing end
- 0000-00-00
- Substance
- HYPOCHLOROUS ACID
- Active strength
- 0 g/.008g
- 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 |
|---|
| 81270-202-01 | PUREHOCL | 500 g in 1 BOTTLE, SPRAY | SPRAY | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81270-202 | PUREHOCL SPRAY [HOCL INC.] | 1 | Legacy NDC, 1 package rows | 20210525_c1799684-8363-27c2-e053-2a95a90aa497.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81270-202-01 | 81270020201 | 500 g in 1 BOTTLE, SPRAY (81270-202-01) | 500 g | 2021-05-01 | 0000-00-00 | No | No | Current |