Gold Edition Ultra Zheng Gu Shui
- Product NDC
- 59321-011
- Requested package NDC
- 59321-011-88
- 11-digit product format
- 593210011
- Labeler code
- 59321
- Product ID
- 59321-011_e7930003-c94f-0deb-e053-2995a90ab67d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol Camphor
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangxi Yulin Pharmaceutical Group Co., Ltd.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-08-31
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (NATURAL); MENTHOL
- Active strength
- 4 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59321-011 | GOLD EDITION ULTRA ZHENG GU SHUI (MENTHOL CAMPHOR) LIQUID [GUANGXI YULIN PHARMACEUTICAL GROUP CO., LTD.] | 1 | Legacy NDC | 20220903_db126904-8858-4094-a2fe-8f23476f2610.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59321-011-88 | 59321001188 | 1 BOTTLE in 1 BOX (59321-011-88) > 88 mL in 1 BOTTLE | 1 bottle | 2022-08-31 | 0000-00-00 | No | No | Current |