Fendall Pure Flow
- Product NDC
- 0498-0630
- 11-digit product format
- 004980630
- Labeler code
- 0498
- Product ID
- 0498-0630_28eea87a-8088-19aa-e063-6394a90aad4a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Purified water
- Dosage form
- LIQUID
- Route
- OPHTHALMIC
- Labeler
- Honeywell Safety Products USA, Inc.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-12-15
- Substance
- WATER
- Active strength
- 98.6 L/100L
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fendall Pure Flow
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WATER | 98.6 L/100L |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 059QF0KO0R |
| Rxcui | 1053173 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0498-0630-37 | Fendall Pure Flow | 14.38 L in 1 CONTAINER | LIQUID | 14.38 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0498-0630 | FENDALL PURE FLOW (PURIFIED WATER) LIQUID [HONEYWELL SAFETY PRODUCTS USA, INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20250207_afda6fc3-7615-b0be-e053-2995a90a6208.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0498-0630-37 | 00498063037 | 14.38 L in 1 CONTAINER (0498-0630-37) | 14.38 l | 2018-12-15 | 0000-00-00 | No | No | Current |