PERSONAL LUBRICANT
- Product NDC
- 81615-001
- 11-digit product format
- 816150001
- Labeler code
- 81615
- Product ID
- 81615-001_c067aaa1-dbbe-a528-e053-2a95a90aebae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM HYALURONATE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Jiangxi Renhetang pharmaceutical chain Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-03-16
- Marketing end
- 0000-00-00
- Substance
- HYALURONATE SODIUM
- Active strength
- 0 g/100mL
- 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 |
|---|
| 81615-001-01 | PERSONAL LUBRICANT | 60 mL in 1 BOTTLE | GEL | 60 | | 5 |
| 81615-001-02 | PERSONAL LUBRICANT | 80 mL in 1 BOTTLE | GEL | 80 | | 5 |
| 81615-001-03 | PERSONAL LUBRICANT | 120 mL in 1 BOTTLE | GEL | 120 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81615-001 | PERSONAL LUBRICANT (SODIUM HYALURONATE) GEL [JIANGXI RENHETANG PHARMACEUTICAL CHAIN CO., LTD.] | 5 | Legacy NDC, 3 package rows | 20210421_bda4df53-00f4-7b00-e053-2a95a90a4227.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81615-001-01 | 81615000101 | 60 mL in 1 BOTTLE (81615-001-01) | 60 ml | 2021-03-16 | 0000-00-00 | No | No | Current |
| 81615-001-02 | 81615000102 | 80 mL in 1 BOTTLE (81615-001-02) | 80 ml | 2021-03-16 | 0000-00-00 | No | No | Current |
| 81615-001-03 | 81615000103 | 120 mL in 1 BOTTLE (81615-001-03) | 120 ml | 2021-03-16 | 0000-00-00 | No | No | Current |