PURECLE
- Product NDC
- 81270-201
- 11-digit product format
- 812700201
- Labeler code
- 81270
- Product ID
- 81270-201_b9379156-1caf-0775-e053-2a95a90ad971
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PURECLE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- HOCL inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-12-01
- 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 |
|---|
| 81270-201-01 | PURECLE | 0.008 g in 1 BOTTLE, SPRAY | SPRAY | 0.008 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81270-201 | PURECLE SPRAY [HOCL INC.] | 2 | Legacy NDC, 1 package rows | 20210119_b8301559-46fb-593e-e053-2a95a90ac634.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81270-201-01 | 81270020101 | .008 g in 1 BOTTLE, SPRAY (81270-201-01) | 2020-12-01 | 0000-00-00 | No | No | Current |