Drugs Similar to PNV-DHA

PNV-DHA + Docusate is a prescription prenatal/postnatal multivitamin/multimineral softgel with DHA. Each softgel is red in color and imprinted with “323” on one side. † Daily Value (DV) not established. SUPPLEMENT FACTS Serving Size: 1 softgel Amount Per Serving % Daily Value Vitamin C (as ascorbic acid, USP) 28 mg 47% Calcium (tribasic calcium phosphate, NF) 160 mg 16% Iron (as ferrous fumarate, USP) 27 mg 150% Vitamin D 3 (as cholecalciferol, USP) 400 IU 100% Vitamin E (as d-alpha-tocopherol acetate, USP) 30 IU 100% Vitamin B 6 (as pyridoxine HCl, USP) 25 mg 1250% Folic Acid, USP 1.25 mg 313% DHA (docosahexaenoic acid) 300 mg † Docusate sodium, USP 55 mg † OTHER INGREDIENTS Bovine Gelatin, Glycerin, Soybean Oil, Soy Lecithin, Purified Water, Yellow Beeswax, FD&C Red # 40, Titanium Dioxide, Orange Cream Flavor, Ethyl Vanillin, FD&C Yellow # 6, and FD&C Blue #1. Contains soy. INDICATIONS PNV-DHA + Docusate is a multivitamin/mineral prescription dietary supplement indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy, and in the postnatal period for both lactating and nonlactating mothers. CONTRAINDICATIONS This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.

take two tablets everty time, two times a day with enough water

take two tablets everty time, two times a day with enough water

Uses: For temporary relief of minor: forgetfulness* dizziness* headache* rash* burning eyes* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS: For temporary relief of tiredness, weakness, general fatigue, exhaustion, and weakness of memory.

Aflora is a prescription multivitamin/multimineral dietary supplement.

INDICATION & USAGE SECTION take two capsules once, two times a day

INDICATIONS & USAGE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

INDICATIONS & USAGE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

INDICATIONS & USAGE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

INDICATIONS & USAGE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

INDICATIONS & USAGE SECTION Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

HOMEOPATHIC INDICATIONS: For the relief of symptoms related to sensitivity to milk or milk products including skin rash, hives, vomiting, bloating, cramping and occasional diarrhea.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INDICATIONS For the temporary relief of itchy, raised, or colored welts on the skin.*

PL Spf indications

AnubisMed 50+ Protection Fluid Indications and Usage

Manufacturer Guangdong Junhui Biotechnology Co., LTD ADDRESS No. 10, Guangrui Street, Guangzhou (Qingyuan) Industrial Transfer Park, Shijiao Town, Qingcheng District, Qingyuan City, Guangdong Province Capacity 130g e 4.5860z Shelf Life 3 Years Place of Origin Made in China

ASCOR (ascorbic acid injection) for intravenous use is a colorless to pale yellow, preservative-free, hypertonic, sterile, non-pyrogenic solution of ascorbic acid. ASCOR must be diluted with an appropriate infusion solution (e.g., 5% Dextrose Injection, USP, Sterile Water for Injection, USP) [see Dosage and Administration (2.1) ] . The chemical name of Ascorbic Acid is L -ascorbic acid. The molecular formula is C 6 H 8 O 6 . It has the following structural formula: Each ASCOR, 50 mL, Pharmacy Bulk Package vial contains 25,000 mg ascorbic acid, equivalent to 28,125 mg sodium ascorbate. Each mL of ASCOR contains 500 mg of ascorbic acid (equivalent to 562.5 mg of sodium ascorbate which amounts to 65 mg sodium/mL of ASCOR), 130 mg of Sodium bicarbonate, and 0.25mg of edetate disodium. Sodium hydroxide is added for pH adjustment (pH range 5.6-6.6). It contains no bacteriostatic or antimicrobial agent. formula

Ascorbic acid injection, USP for intravenous use is a colorless to pale yellow, preservative-free, hypertonic, sterile, non-pyrogenic solution of ascorbic acid. Ascorbic acid injection must be diluted with an appropriate infusion solution (e.g., 5% Dextrose Injection, USP; Sterile Water for Injection, USP) [see Dosage and Administration (2.1) ] . The chemical name of ascorbic acid, USP is L -ascorbic acid. The molecular formula is C 6 H 8 O 6 . It has the following structural formula: Each ascorbic acid injection, USP, 50 mL, Pharmacy Bulk Package vial that contains 25,000 mg ascorbic acid, equivalent to 28,125 mg sodium ascorbate. Each mL of ascorbic acid injection, USP contains 500 mg of ascorbic acid (equivalent to 562.5 mg of sodium ascorbate which amounts to 65 mg sodium/mL of ascorbic acid injection), 130 mg of sodium bicarbonate 0.28 mg of edetate disodium (dihydrate). Sodium hydroxide is added for pH adjustment (pH range 5.6 to 6.6). It contains no bacteriostatic or antimicrobial agent. Structural formula of Ascorbic Acid

Directions: FOR ORAL USE ONLY.

INDICATIONS For the temporary relief of anxiousness, difficulty concentrating, irritability, sadness, dry or irritated skin, difficulty falling asleep or restlessness, or occasional headache.*