Multi-Vitamin Drops with Fluoride and Iron NDC 58657-327

NDC codes

FDA NDC Directory

Product NDC (as listed)58657-327Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58657-0327Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
58657-327-50	58657032750	1 BOTTLE, DROPPER in 1 BOX (58657-327-50) / 50 mL in 1 BOTTLE, DROPPERMarketed from Feb 24, 2017

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Multi-Vitamin Drops with Fluoride and Iron
Generic name (nonproprietary): vitamin a, ascorbic acid, cholecalciferol, alpha-tocopherol acetate, thiamine hydrochloride, riboflavin 5-phosphate sodium, niacinamide, pyridoxine hydrochloride, ferrous sulfate and sodium fluoride
Active ingredients: Vitamin a palmitate — 1500 [iU]/mLAscorbic acid — 35 mg/mLCholecalciferol — 400 [iU]/mL.alpha.-tocopherol succinate, D- — 5 [iU]/mLThiamine hydrochloride — .5 mg/mLRiboflavin 5'-phosphate sodium — .6 mg/mLNiacinamide — 8 mg/mLPyridoxine hydrochloride — .4 mg/mLFerrous sulfate — 10 mg/mLSodium fluoride — .25 mg/mL
Dosage form: Liquid
Route: Oral
Labeler: Method Pharmaceuticals, LLC
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Feb 24, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Photoabsorption (Mechanism)Photosensitizing Activity (Physiologic effect)Vitamin A (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)
Identifiers: Product ID 58657-327_41b5d787-acb5-89e9-e063-6294a90aa957SPL ID 41b5d787-acb5-89e9-e063-6294a90aa957SPL set ID d5609742-e456-4409-bca9-706b0ea90d35UNII 1D1K0N0VVC, PQ6CK8PD0R, 1C6V77QF41, LU4B53JYVE, M572600E5P, 20RD1DZH99, 25X51I8RD4, 68Y4CF58BV, 39R4TAN1VT, 8ZYQ1474W7
Pharmacologic class: Photoenhancer; Vitamin A; Vitamin B6 Analog; Vitamin C; Vitamin D

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N458657032750 followed by a unit qualifier and the quantity

Package 58657-0327-50. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 21, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Supplementation of the diet with vitamins A, C and D. Multi-Vitamin Drops with Fluoride and Iron 0.25 mg also provides fluoride for caries prophylaxis. The American Academy of Pediatrics recommends that children up to age 16, in areas where drinking water contains less than optimal levels of fluoride, receive daily fluoride supplementation. The American Academy of Pediatrics recommend that infants and young children 6 months to 3 years of age, in areas where the drinking water contains less than 0.3 ppm of fluoride, and children 3-6 years of age, in areas where the drinking water contains 0.3 through 0.6 ppm of fluoride, receive 0.25 mg of supplemental fluoride daily wh…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)