Home FDA labels 41b5fe6c-faec-bbbb-e063-6294a90a7549 Multivitamin with Fluoride openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Multivitamin with Fluoride
Generic name .ALPHA.-TOCOPHEROL ACETATE, DL-, ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D
Manufacturer Method Pharmaceuticals, LLC
Product type HUMAN PRESCRIPTION DRUG
SPL set ID 42ed15a5-aad6-4ab3-b95b-f9534a419f40
SPL ID 41b5fe6c-faec-bbbb-e063-6294a90a7549
Version 12
Effective date 2025-10-21
Source export date 2026-09-28
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:28:14 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Multivitamin with Fluoride openfda.brand_name generic name .ALPHA.-TOCOPHEROL ACETATE, DL-, ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D openfda.generic_name manufacturer name Method Pharmaceuticals, LLC openfda.manufacturer_name ndc package 58657-163-90 openfda.package_ndc ndc package 58657-163-01 openfda.package_ndc ndc product 58657-163 openfda.product_ndc ndc11 package 58657016301 derived:openfda.package_ndc ndc11 package 58657016390 derived:openfda.package_ndc spl id 41b5fe6c-faec-bbbb-e063-6294a90a7549 id spl set id 42ed15a5-aad6-4ab3-b95b-f9534a419f40 set_id unii 2679MF687A openfda.unii unii TLM2976OFR openfda.unii unii 8ZYQ1474W7 openfda.unii unii 935E97BOY8 openfda.unii unii PQ6CK8PD0R openfda.unii unii 81G40H8B0T openfda.unii unii P6YC3EG204 openfda.unii unii 8K0I04919X openfda.unii unii WR1WPI7EW8 openfda.unii unii KV2JZ1BI6Z openfda.unii unii 9VU1KI44GP openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNING Keep out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. CAUTION Do not eat or drink dairy products within one hour of fluoride administration. Should be chewed. This product, as all chewable tablets, is not recommended for children under age 4 due to risk of choking.
Adverse reactions cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions sections page 1 of 1 · 1 matching rows.
adverse reactions ADVERSE REACTIONS Allergic rash and other idiosyncrasies have been rarely reported.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.