说明与适用边界
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spl product data elements
Guardian Ultra Strength Antacid Assorted Fruit Calcium carbonate CALCIUM CARBONATE CALCIUM CATION ADIPIC ACID STARCH, CORN CROSPOVIDONE DEXTROSE, UNSPECIFIED FORM FD&C BLUE NO. 1 ALUMINUM LAKE MAGNESIUM STEARATE MALTODEXTRIN SUCROSE TALC D&C RED NO. 27 ALUMINUM LAKE D&C RED NO. 30 D&C YELLOW NO. 10 FD&C YELLOW NO. 6 reddish pink G171
活性成分 / Active ingredient
ACTIVE INGREDIENT (in each tablet) Calcium carbonate 1000 mg
用途 / Purpose
PURPOSE Antacid
适应证 / Indications and usage
USE(S) relieves: acid indigestion heartburn
警告 / Warnings
WARNINGS .
咨询医药人员 / Ask a doctor or pharmacist
ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE presently taking a prescription drug. Antacids may interact with certain prescription drugs.
使用中 / When using
WHEN USING THIS PRODUCT do not take more than 7 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.
孕哺期 / Pregnancy or breastfeeding
IF PREGNANT OR/BREASTFEEDING, ask a health professional before use.
儿童安全 / Keep out of reach of children
KEEP OUT OF REACH OF CHILDREN .
用法用量原文 / Dosage and administration
DIRECTIONS adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor.
储存 / Storage and handling
OTHER INFORMATION each tablet contains: elemental calcium 400 mg do not use if printed seal under cap is torn or missing. store at room temperature. Keep the container tightly closed.
辅料 / Inactive ingredients
INACTIVE INGREDIENTS adipic acid, corn starch, crospovidone, D&C red 27 lake, D&C red 30 lake, D&C yellow 10 lake, dextrose, FD&C blue 1 lake, FD&C yellow 6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc.
package label principal display panel
PRINCIPAL DISPLAY PANEL *Compare to the active ingredient in Tums® Ultra Strength GUARDIAN® NDC 53041-171-68 Ultra Strength Alkums Antacid Tablets Assorted Fruit Flavors Calcium Carbonate 1000 mg Relieves: Acid Indigestion Heartburn 72 CHEWABLE TABLETS 171-72-gdc.jpg
来源、版本与许可
- 资料类型
- 美国药品标签原文
- 版本
- 1 / 20240429
- 获取时间
- 2026-10-08
- 许可
- openFDA public data; retain original label attribution. See 查看来源 and dataset source notices. Public access does not imply approval or unrestricted rights to every submitted label.

