Iodo Blanco (Iodine Tincture Decolorized)
- Product NDC
- 73635-1222
- 11-digit product format
- 736351222
- Labeler code
- 73635
- Product ID
- 73635-1222_40a7584f-3b4f-a0c7-e063-6294a90a586e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Iodine 2%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Germa Products, LLC
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-29
- Substance
- IODINE
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Iodo Blanco (Iodine Tincture Decolorized)
- Brand name suffix
- First Aid Antiseptic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IODINE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9679TC07X4 |
| Rxcui | 311093 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73635-1222-1 | Iodo Blanco (Iodine Tincture Decolorized)First Aid Antiseptic | 30 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 30 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73635-1222 | IODO BLANCO (IODINE TINCTURE DECOLORIZED) FIRST AID ANTISEPTIC (IODINE 2%) LIQUID [GERMA PRODUCTS, LLC] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241017_bf54254f-2ef3-102e-e053-2995a90ac083.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 |
|---|
| 73635-1222-1 | 73635122201 | 30 mL in 1 BOTTLE, WITH APPLICATOR (73635-1222-1) | 30 ml | 2021-03-29 | 0000-00-00 | No | No | Current |