United States · FDA National Drug Code directory

Reflux Away

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
70163-0041_f2450c84-42d4-4f78-9884-86febc04bef2
Product NDC
70163-0041
Form
TABLET
Composition / generic term
Abies Nigra, Antimonium Crudum, Argentum Nitricum, Carbo Vegetabilis, Chelidonium Majus, Colocynthis, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica
Labeler
NaturalCare
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20260324
Source listing expiry
20271231

Source-listed ingredients

  • PICEA MARIANA RESIN — 6 [hp_Q]/1
  • ANTIMONY TRISULFIDE — 12 [hp_X]/1
  • SILVER NITRATE — 6 [hp_X]/1
  • ACTIVATED CHARCOAL — 12 [hp_X]/1
  • CHELIDONIUM MAJUS WHOLE — 3 [hp_X]/1
  • CITRULLUS COLOCYNTHIS FRUIT PULP — 6 [hp_X]/1
  • LYCOPODIUM CLAVATUM SPORE — 3 [hp_X]/1
  • SODIUM CHLORIDE — 6 [hp_X]/1
  • STRYCHNOS NUX-VOMICA SEED — 3 [hp_X]/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (70163-0041-1) / 60 TABLET in 1 BLISTER PACK · 70163-0041-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →