Kelife Iodine Norwegian Seaweed
by Douglas Laboratories · tablet or pill · 100 tablets
- Off the market since June 2020 (NIH)
- UPC 3 10539 01288 8
- DSLD label 56039
- Serving 1 tablet
- 100 servings
Kelife Iodine Norwegian Seaweed by Douglas Laboratories lists 2 ingredients, 2 with an amount per serving of 1 tablet, such as 250 mcg of iodine and 500 mg of norwegian seaweed. Its current label entered the NIH Dietary Supplement Label Database on January 25, 2016.
What is in Kelife Iodine Norwegian Seaweed?
Each row as the label prints it, per serving of 1 tablet. The capsule beside an amount places it among every product in the NIH database that lists the same ingredient: the bar is the middle half of their amounts, the line in it the median, the whiskers the 10th and 90th percentiles; the green tick is the FDA Daily Value and the red dashed tick the adult upper limit (IOM).
| Ingredient | Amount | % DV | Among products listing it |
|---|---|---|---|
| Iodineas SeaweedIodine (Form: sourced from Norwegian Seaweed) | 250 mcg | 167% | Higher than 93% of 6,382 products listing iodine (median 150 mcg). |
| Norwegian Seaweed | 500 mg | Higher than 81% of 54 products listing ascophyllum nodosum (median 100 mg). |
Source: NIH ODS Dietary Supplement Label Database, label 56039 (entered January 25, 2016), version 9.4.0. See the label on DSLD. Amounts are what the maker printed; DSLD does not test products. Daily Values: the FDA's Daily Value page.
Is that a lot?
The rows in the top or bottom tenth of the products that list the same ingredient, and any above the adult upper limit at the most servings a day the directions give:
- Its 250 mcg of iodine is higher than 93% of the 6,382 iodine products that print an amount; 396 list more.
The NIH database records one serving a day from the label's directions; its % Daily Values are for adults and children 4 or more years of age. The directions as printed are further down this page.
The Tolerable Upper Intake Level is the most of a nutrient per day, from food, water and supplements together, that is likely to pose no risk for almost all adults (Institute of Medicine, 2011). It does not apply under medical supervision. This page compares labels; it is not medical advice.
Sources: amounts from the DSLD label; Daily Values from 21 CFR 101.9(c)(8)(iv); adult upper limits from the Institute of Medicine's DRI summary tables (2011). How positions are computed.
Which products have the closest formulas?
6 products list the very same ingredients; the nearest amounts come first.
- Kelife Norwegian SeaweedDouglas Laboratories · off the market same ingredients
- Kelife IodineDouglas Laboratories same ingredients
- KelpThymely Solutions same ingredients
- KelpOregon's Wild Harvest same ingredients
- KelpEndo-met Laboratories same ingredients
- Kelp ThallusNature's Answer same ingredients
Source: ingredient lists of every product's current label in DSLD (version 9.4.0); similarity weights each shared ingredient by how rare it is.
What does the label say about taking it?
Quoted from the label as DSLD transcribed it: the maker's words, including any claim about what the product does, which the FDA has not evaluated and PlainVitamins does not endorse.
- Directions
- Suggested Usage: As a dietary supplement, adults take 1 tablet daily or as directed by your healthcare professional. This product is best taken with meals.
- Warnings
- KEEP OUT OF REACH OF CHILDREN.
- Tamper resistant package, do not use if outer seal is missing.
- Allergens and what it does not contain
- This product contains NO yeast, wheat, gluten, soy, milk/dairy, corn, sodium, sugar, starch, artificial coloring, artificial preservatives or genetically modified organisms (GMOs).
- Storage
- For optimal storage conditions, store in a cool, dry place. (59(0)-77(0)F/15(0)-25(0)C) (35-65% relative humidity)
Source: label statements in DSLD label 56039.
What else is on the label?
Other ingredients: Dicalcium Phosphate, Cellulose, Povidone, Vegetable Stearate, Silica.
How many labels does Kelife Iodine Norwegian Seaweed have?
One label is on file, entered on January 25, 2016.
- Label 56039 (current) Entered January 25, 2016 · off the market June 26, 2020 · 100 tablets · UPC 3 10539 01288 8
Source: DSLD label entry and market events, version 9.4.0 (labels entered through September 25, 2025).
Who makes it?
The label names Douglas Laboratories (manufacturer), Pittsburgh, PA. All Douglas Laboratories products.