OB Towelette
- Product NDC
- 50730-5102
- 11-digit product format
- 507305102
- Labeler code
- 50730
- Product ID
- 50730-5102_4f082dc2-bac8-4d2c-901f-381c65c2e7cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- H and P Industries, Inc. dba Triad Group
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1999-07-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mL/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50730-5102-0 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-dac1-621f-e053-dbdaa90a74ad | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50730-5102-0 | OB Towelette | 1 in 1 POUCH | SOLUTION | 1 | 1 | |
| 50730-5102-0 | OB Towelette | 100 in 1 CARTON | SOLUTION | 100 | 1 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| benzalkonium chloride | ACTIVE INGREDIENT | F5UM2KM3W7 | OB TOWELETTE (BENZALKONIUM CHLORIDE) SOLUTION [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 | |
| benzalkonium | ACTIVE MOIETY | 7N6JUD5X6Y | OB TOWELETTE (BENZALKONIUM CHLORIDE) SOLUTION [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 | |
| sodium bicarbonate | INACTIVE INGREDIENT | 8MDF5V39QO | OB TOWELETTE (BENZALKONIUM CHLORIDE) SOLUTION [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | OB TOWELETTE (BENZALKONIUM CHLORIDE) SOLUTION [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50730-5102 | OB TOWELETTE (BENZALKONIUM CHLORIDE) SOLUTION [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 | Legacy NDC, 2 package rows | 20091202_60a3aa8b-d16b-4368-8fab-d613c4e7ee5a.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1038561 | benzalkonium Cl 0.4 % Medicated Pad | PSN | 60a3aa8b-d16b-4368-8fab-d613c4e7ee5a | 1 |
| 1038561 | benzalkonium chloride 4 MG/ML Medicated Pad | SCD | 60a3aa8b-d16b-4368-8fab-d613c4e7ee5a | 1 |
| 1038561 | benzalkonium chloride 0.4 % Medicated Towelette | SY | 60a3aa8b-d16b-4368-8fab-d613c4e7ee5a | 1 |
| 1038561 | benzalkonium chloride 0.4 % Topical Swab | SY | 60a3aa8b-d16b-4368-8fab-d613c4e7ee5a | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 50730-5102-0 | 50730510200 | 1 in 1 POUCH | Historical |