D-d Sudium Bicarbonate U.s.p. Powder
Product Images NDC 84178-105

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for D-d Sudium Bicarbonate U.s.p. (NDC 84178-105). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Evi Labs, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label 16 Oz (D D Sodium Bicarbonate 16 Oz)

Label 16 Oz (D   D Sodium Bicarbonate 16 Oz)
Drug Facts panel for D-D Sodium Bicarbonate U.S.P. Bicarbonato De Soda Puro powder. Active ingredient is 100% sodium bicarbonate as an antacid. Includes uses, warnings, directions for adults and children, storage instructions, and contact information for A.G. Marin Pharmaceuticals. Tamper-evident disclosure and barcode are also shown.*
FDA Label Image

Label 8 Oz (D D Sodium Bicarbonate 8 Oz)

Label 8 Oz (D   D Sodium Bicarbonate 8 Oz)
Label for D-D Sodium Bicarbonate U.S.P. (Bicarbonato de Soda Puro) oral powder, 315 mg/g strength. The label includes Drug Facts with active ingredient sodium bicarbonate, uses for heartburn and indigestion relief, warnings, directions for use, storage information, and manufacturer details from A.G. Marin Pharmaceutical. Net weight is 8 oz. The label is primarily blue and white with bilingual English and Spanish text.*
FDA Label Image

Principal Display Panel (D D Sodium Bicarbonate 4 Oz)

Principal Display Panel (D  D Sodium Bicarbonate 4 Oz)
Drug Facts panel for D & D Sodium Bicarbonate U.S.P. powder, showing active ingredient sodium bicarbonate U.S.P. 100% with antacid purpose. It details uses for relief of heartburn and upset stomach, warnings including dosage limits and sodium restriction advice, directions for use, storage instructions, inactive ingredients noted as none, and a tamper-evident disclosure. Manufacturer contact and barcode are also visible.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.