Cyberderm
- Product NDC
- 71644-003
- Requested package NDC
- 71644-003-50
- 11-digit product format
- 716440003
- Labeler code
- 71644
- Product ID
- 71644-003_f1ffd54f-186a-32e0-e053-2a95a90a2e09
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cyberderm Laboratories Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-03-30
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 25 g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71644-003 | CYBERDERM SIMPLY ZINC ULTRA (ZINC OXIDE) LOTION [CYBERDERM LABORATORIES INC.] | 5 | Legacy NDC | 20231128_69085599-01a5-1c83-e053-2991aa0a3432.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71644-003-50 | 71644000350 | 1 BOTTLE in 1 CARTON (71644-003-50) > 50 mL in 1 BOTTLE | 1 bottle | 2018-03-30 | 0000-00-00 | No | No | Current |