Zinc Oxide
- Product NDC
- 42213-365
- 11-digit product format
- 422130365
- Labeler code
- 42213
- Product ID
- 42213-365_b4c9e519-4ee3-4cba-9338-148b9cade2ac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Ultra Seal Corporation
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-05-03
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 200 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42213-365-48 | 42213036548 | 1 TUBE in 1 CARTON (42213-365-48) > 56 g in 1 TUBE (42213-365-56) | 1 tube | 2012-05-03 | 0000-00-00 | No | No | Current |