Doxy 100(tm) Doxycycline Injection, Powder, Lyophilized, For Solution
Product Images NDC 51662-1402

9 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Doxy 100(tm) Doxycycline (NDC 51662-1402). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

51662 1402 2 Pouch Hf Label Image

51662 1402 2 Pouch Hf Label Image
Label for DOXY 100(TM) DOXYCYCLINE injection powder, lyophilized, for solution. The vial contains 100 mg per 20 mL and is intended for intravenous use. Manufactured by HF Acquisition Co LLC, DBA HealthFirst, Mukilteo, WA. The label includes NDC 51662-1402-2, lot number, and expiration date, with storage and handling instructions.*
FDA Label Image

51662 1402 3 Rfid Serialized Labeling

51662 1402 3 Rfid Serialized Labeling
DOXY 100(TM) DOXYCYCLINE 100 mg/10mL injection powder, lyophilized for solution is shown in a partial label image. The label includes a barcode, numeric identifiers, and distributor information indicating HF Acquisition Co LLC, DBA HealthFirst, Mukilteo, WA.*
FDA Label Image

51662 1402 3 Serialized Box Labeling

51662 1402 3 Serialized Box Labeling
Label for DOXY 100(TM) Doxycycline for Injection, USP, 100 mg per 20 mL vial, box of 10. The label includes NDC 51662-1402-3, lot and expiration dates, and storage instructions. It states the product is preservative free, sterile, lyophilized for intravenous infusion, requiring further dilution after reconstitution. Manufactured by HF Acquisition Co LLC, Mukilteo, WA.*
FDA Label Image
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table showing product code, unit of sale, strength, and packaging details for doxycycline solution. It lists product code 1311, unit of sale as NDC 63323-130-11, strength as doxycycline hyclate equivalent to 100 mg doxycycline per vial, and packaging as a 20 mL single dose vial with NDC 63323-130-02.*
FDA Label Image

Serialized Vial Labeling (Serialized Vial Labeling)

Serialized Vial Labeling (Serialized Vial Labeling)
DOXY 100 TM Doxycycline injection powder vial for intravenous use in a brown glass container with an orange and white label. The label indicates 100 mg per vial strength and specifies that the product must be further diluted after reconstitution. The vial has a silver and orange cap, with additional labeling including a QR code and distributor information from HF Acquisition Co LLC, DBA HealthFirst.*
FDA Label Image

S2 (Structure 2)

S2 (Structure 2)
Chemical formula table showing the molecular composition of doxycycline: (C22H24N2O8 • HCl)2 • C2H6O • H2O with a molecular weight of 1025.89.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of doxycycline for DOXY 100(TM) DOXYCYCLINE injection, showing the molecular arrangement including hydroxyl, ketone, and amide groups, as well as associated hydrochloride, water, and ethanol molecules.*
FDA Label Image

Vial Label (Vial Label)

Vial Label (Vial Label)
Label for DOXY 100 DOXYCYCLINE injection powder, lyophilized for solution, 100 mg per vial. The label states it is for intravenous infusion only, preservative free, and must be further diluted after reconstitution. Storage conditions and protection from light are noted. Manufactured by HF Acquisition Co LLC, DBA HealthFirst, with NDC 63323-130-11.*

* 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.