Iodo Albo Iodide
- Manufacturer
- Menper Distributors Inc.
- Effective date
- 2020-02-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:03:40
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
DOSAGE & ADMINISTRATION SECTION
Clean the affected area, apply a small amount on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.
OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 48%
INDICATIONS & USAGE SECTION
First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns.
WARNINGS SECTION
For External Use Only.
When using this product:
Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns consult a doctor.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately. Soap will deactivate the effects of this product.
INACTIVE INGREDIENT SECTION
- Ammonium Hydroxide
- Iodine
- Potassium Iodide
- Purified Water
OTC - PURPOSE SECTION
First Aid Antiseptic
Iodo Albo Iodide
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5f30b278-5791-4113-8781-878a9221ef8a | Product name | 2 | 20230125 |
| 2a70c781-a755-4d76-b20a-a958acfbdcdc | Product name | 2 | 20190619 |
| 304592ef-4a8a-4c22-8e8c-af73aa3d60e5 | Product name | 1 | 20180703 |
| ac0821a1-ce75-4ea7-880a-59eecaecdf22 | Product name | 1 | 20180703 |
| db5dc4f9-b907-46f6-8fb7-babcf04bbe5c | Product name | 1 | 20180619 |
| 41e9d6cf-3ed7-4c44-a57e-0685058d0896 | Product name | 1 | 20170824 |
| 5e652c92-68fd-426b-b0e7-5fc64e0b9f99 | Product name | 1 | 20170309 |
| ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c | Product name | 1 | 20150421 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 53145-120-91 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-b3b1-d8a0-e053-dadaa90a6e4e | Iodo Albo Iodide |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53145-120-91 | Iodo Albo Iodide | 30 mL in 1 CONTAINER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Iodo Albo Iodide
- Alcohol Liquid
- IODINE
- POTASSIUM IODIDE
- AMMONIA
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53145-120 | 53145-120-91 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| IODINE | 9679TC07X4 | IACT |
| POTASSIUM IODIDE | 1C4QK22F9J | IACT |
| AMMONIA | 5138Q19F1X | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 9e3066b1-5bca-a5c9-e053-2a95a90a5e80 | 9e30a6a5-324b-5619-e053-2995a90a8ba0 | 2020-02-09 | Warnings | 9e3066b1-5bca-a5c9-e053-2a95a90a5e80 9e30a6a5-324b-5619-e053-2995a90a8ba0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
