SURVIVEX TRAVEL MED MOD- convenience kit kit
Drug Labeling and Warnings
Drug Details [pdf]
- WARNINGS
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SURVIVEX TRAVEL MED MOD
convenience kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 87625-200 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 87625-200-01 1 in 1 KIT; Type 0: Not a Combination Product 05/18/2026 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 4 Part 2 4 Part 3 4 Part 4 5 Part 5 3 Part 6 3 Part 7 3 Part 8 3 Part 9 3 Part 10 3 Part 11 4 Part 1 of 11 MEDI-FIRST IBUPROFEN
ibuprofen tablet, coatedProduct Information Item Code (Source) NDC: 87625-113(NDC:47682-700) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color red (Reddish Brown) Score no score Shape ROUND Size 10mm Flavor Imprint Code G;2 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA079174 01/26/2017 Part 2 of 11 MEDI-FIRST NON ASPIRIN
acetaminophen tablet, coatedProduct Information Item Code (Source) NDC: 87625-102(NDC:47682-803) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white (white) Score no score Shape ROUND (Round) Size 10mm Flavor Imprint Code AZ;234 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 03/27/2024 Part 3 of 11 MEDI-FIRST ASPIRIN
aspirin tablet, film coatedProduct Information Item Code (Source) NDC: 87625-103(NDC:47682-617) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white Score no score Shape ROUND Size 10mm Flavor Imprint Code 44;157;ASPIRIN Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 07/20/2020 Part 4 of 11 MEDI-FIRST ANTACID
calcium carbonate tablet, chewableProduct Information Item Code (Source) NDC: 87625-105(NDC:47682-820) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 420 mg Inactive Ingredients Ingredient Name Strength MALTODEXTRIN (UNII: 7CVR7L4A2D) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 11mm Flavor Imprint Code AZ;036 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 06/15/2014 Part 5 of 11 MEDIQUE MEDI-SELTZER
aspifin tablet, effervescent tablet, effervescentProduct Information Item Code (Source) NDC: 87625-115(NDC:47682-147) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Product Characteristics Color white Score no score Shape ROUND Size 25mm Flavor Imprint Code L421 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 03/17/2025 Part 6 of 11 MEDIQUE DIAMODE
loperamide hydrochloride tabletProduct Information Item Code (Source) NDC: 87625-107(NDC:47682-200) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LOPERAMIDE HYDROCHLORIDE (UNII: 77TI35393C) (LOPERAMIDE - UNII:6X9OC3H4II) LOPERAMIDE HYDROCHLORIDE 2 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color green (green) Score 2 pieces Shape OVAL (Caplet) Size 10mm Flavor Imprint Code 123 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA074091 12/30/2008 Part 7 of 11 MEDIQUE MEDI-MECLIZINE
meclizine hydrochloride tabletProduct Information Item Code (Source) NDC: 87625-108(NDC:47682-481) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO) (MECLIZINE - UNII:3L5TQ84570) MECLIZINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color yellow Score no score Shape ROUND Size 9mm Flavor Imprint Code 44;403 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M009 12/14/2020 Part 8 of 11 MEDI-FIRST SINUS DECONGESTANT
phenylephrine hydrochloride tablet, film coatedProduct Information Item Code (Source) NDC: 87625-109(NDC:47682-809) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color red (red) Score no score Shape ROUND (ROUND) Size 7mm Flavor Imprint Code 272 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/21/2026 Part 9 of 11 MEDIQUE LORADAMED
loratadine tablet, film coatedProduct Information Item Code (Source) NDC: 87625-110(NDC:47682-203) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color white (white) Score no score Shape ROUND (ROUND) Size 6mm Flavor Imprint Code RX;526 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076134 12/30/2008 Part 10 of 11 MEDIQUE DIPHEN
diphenhydramine hydrochloride tablet, film coatedProduct Information Item Code (Source) NDC: 87625-111(NDC:47682-167) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color pink (pink) Score no score Shape OVAL (OVAL) Size 11mm Flavor Imprint Code 048;D Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 01/01/2012 Part 11 of 11 MEDIQUE DIOTAME
bismuth subsalicylate tablet, chewableProduct Information Item Code (Source) NDC: 87625-114(NDC:47682-210) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ, BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE 262 mg Inactive Ingredients Ingredient Name Strength ASPARTAME (UNII: Z0H242BBR1) Product Characteristics Color pink Score no score Shape ROUND Size 16mm Flavor PEPPERMINT Imprint Code RH;046 Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 04/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 05/18/2026 Labeler - Intent Brands LLC (129848781) Registrant - Intent Brands LLC (129848781) Establishment Name Address ID/FEI Business Operations Intent Brands LLC 129848781 manufacture(87625-200)
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