Maximum Strength Moisture Barrier
- Product NDC
- 64772-203
- 11-digit product format
- 647720203
- Labeler code
- 64772
- Product ID
- 64772-203_41ee91c0-d197-cc0f-e063-6394a90a7b97
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petrolatum and Zinc Oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Derma Sciences Canada Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-11-13
- Substance
- PETROLATUM; ZINC OXIDE
- Active strength
- .5; .16 g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Maximum Strength Moisture Barrier
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PETROLATUM | .5 g/g |
| ZINC OXIDE | .16 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4T6H12BN9U, SOI2LOH54Z |
| Rxcui | 2727316 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64772-203-01 | Maximum Strength Moisture Barrier | 113.4 g in 1 TUBE | OINTMENT | 113.4 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 64772-203-01 | 64772020301 | 113.4 g in 1 TUBE (64772-203-01) | 113.4 g | 2014-11-13 | No | No | Historical |