KINLO ALWAYS GOLDEN BODY
- Product NDC
- 82184-1001
- Requested package NDC
- 82184-1001-3
- 11-digit product format
- 821841001
- Labeler code
- 82184
- Product ID
- 82184-1001_dac29445-e3b7-95ff-e053-2a95a90a43de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- A-Frame SunCo Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-02-28
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 10 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82184-1001 | KINLO ALWAYS GOLDEN BODY (ZINC OXIDE) LOTION [A-FRAME SUNCO INC] | 3 | Legacy NDC | 20241229_d91e9ef3-1581-c362-e053-2a95a90ad57a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82184-1001-3 | 82184100103 | 170 g in 1 TUBE (82184-1001-3) | 170 g | 2022-02-28 | 0000-00-00 | No | No | Current |