ProCure SkinGuard
- Product NDC
- 55681-030
- 11-digit product format
- 556810030
- Labeler code
- 55681
- Product ID
- 55681-030_3ac23056-720f-eca5-e063-6394a90a8cc7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petrolatum 49.9%
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Twin Med LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-07-17
- Substance
- PETROLATUM
- Active strength
- 49.9 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ProCure SkinGuard
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PETROLATUM | 49.9 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4T6H12BN9U |
| Rxcui | 2719616 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55681-030-04 | ProCure SkinGuard | 99.2 g in 1 TUBE | OINTMENT | 99.2 | | 3 |
| 55681-030-05 | ProCure SkinGuard | 5 g in 1 PACKET | OINTMENT | 5 | | 3 |
| 55681-030-07 | ProCure SkinGuard | 198 g in 1 TUBE | OINTMENT | 198 | | 3 |
| 55681-030-14 | ProCure SkinGuard | 144 in 1 CARTON | OINTMENT | 144 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-030-04 | 55681003004 | 99.2 g in 1 TUBE (55681-030-04) | 99.2 g | 2025-07-17 | No | No | Current |
| 55681-030-05 | 55681003005 | 5 g in 1 PACKET | 5 g | | | | Historical |
| 55681-030-07 | 55681003007 | 198 g in 1 TUBE (55681-030-07) | 198 g | 2025-07-17 | No | No | Current |
| 55681-030-14 | 55681003014 | 144 PACKET in 1 CARTON (55681-030-14) / 5 g in 1 PACKET (55681-030-05) | 144 packet | 2025-07-17 | No | No | Current |