ProCure SkinGuard
- Product NDC
- 55681-077
- 11-digit product format
- 556810077
- Labeler code
- 55681
- Product ID
- 55681-077_5cb4ae80-cf37-3b3d-e063-6294a90a54f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petrolatum and Zinc Oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Twin Med LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-29
- Substance
- ZINC OXIDE; PETROLATUM
- Active strength
- 2; 49.9 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ProCure SkinGuard
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC OXIDE | 2 g/100g |
| PETROLATUM | 49.9 g/100g |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 55681-077-14 | 55681007714 | 144 PACKET in 1 CARTON (55681-077-14) / 5 g in 1 PACKET (55681-077-05) | 144 packet | 2026-09-30 | No | No | Current |
| 55681-077-35 | 55681007735 | 99.2 g in 1 TUBE (55681-077-35) | 99.2 g | 2026-09-30 | No | No | Current |