FDA.reportPublic FDA data

NDC 87625-101 - SurviveX Travel Med Kit

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
87625-101
Manufacturer
Intent Brands LLC
Effective date
2026-05-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SurviveX Travel Med Kit - Intent Brands LLCIntent Brands LLC2026-05-07HUMAN OTC DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 310 of 472 · 9,427 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetaminophenACETAMINOPHENCVS Pharmacy6f880abe-5284-42b0-9db6-b071444b197b2024-12-27WarningsExact identifier
unii: 362O9ITL9D
LoratadineLORATADINEPremier Valuedc22862e-fe91-4900-8c2b-1ca45aeedbf02024-12-27WarningsExact identifier
unii: 7AJO3BO7QN
CHILDRENS LORATADINELORATADINETARGET CORPORATIONc02ad905-2363-4092-a90e-3be789112cb12024-12-27WarningsExact identifier
unii: 7AJO3BO7QN
Childrens AllergyLORATADINETARGET CORPORATION9507c223-ea75-477e-b765-f5d0bcba5ff92024-12-27WarningsExact identifier
unii: 7AJO3BO7QN
SDA Laboratories TussinGUAIFENESINSDA Laboratories, Inc.2a444cc8-96be-9432-e063-6394a90a1b632024-12-27WarningsExact identifier
application number: M012
SDA Laboratories Tussin DMDEXTROMETHORPHAN HBR, GUAIFENESINSDA Laboratories, Inc.2a445f31-818d-11b1-e063-6294a90a8cb12024-12-27WarningsExact identifier
application number: M012
AllervarxLORATADINEInnovus Pharmaceuticals, Inc.ec4d1e77-6995-4228-8e63-a9ab6232dace2024-12-27WarningsExact identifier
unii: 7AJO3BO7QN
AllervarxLORATADINEInnovus Pharmaceuticals, Inc.885e81ae-5ea3-4d14-8666-8c26987670142024-12-27WarningsExact identifier
unii: 7AJO3BO7QN
Bi-Mart Extra Strength Antacid Assorted BerryCALCIUM CARBONATEBi-Mart0d50c08a-833f-4821-a2ed-7801b885706f2024-12-26WarningsExact identifier
application number: M001
unii: H0G9379FGK
IbuprofenIBUPROFENAurohealth LLC09bd3935-526d-4ad1-898a-4f0d9499ebb92024-12-26WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
AcetaminophenACETAMINOPHENCHAIN DRUG MARKETING ASSOCIATION INC.1608b4f0-bf20-4024-b8f2-20a4df7a4b212024-12-26WarningsExact identifier
application number: M013
unii: 362O9ITL9D
Regular Strength Antacid MintALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONETopco Associates, LLC59c16c09-c23d-4a37-8460-d6c00a268ed52024-12-26WarningsExact identifier
application number: M001
BI-MART Ultra Strength Antacid PeppermintCALCIUM CARBONATEBi-Mart071cab57-13c8-40b6-a891-9d0ef54034e82024-12-26WarningsExact identifier
application number: M001
unii: H0G9379FGK
Aacetaminophen and IbuprofenACETAMINOPHEN AND IBUPROFENGRANULES USA, INC.1dd90684-6505-8e07-e063-6394a90afdf42024-12-26WarningsExact identifier
unii: WK2XYI10QM
unii: 362O9ITL9D
ANTACIDCALCIUM CARBONATEAdvance Pharmaceutical Inc.face4e8c-3d0f-4c2e-83c1-44397b225ae72024-12-26WarningsExact identifier
application number: M001
unii: H0G9379FGK
AspirinASPIRINAdvance Pharmaceutical Inc.f6a9ea44-08b8-4a33-bfbd-68cb2d852c392024-12-26WarningsExact identifier
application number: M013
unii: R16CO5Y76E
ANTACIDCALCIUM CARBONATEAdvance Pharmaceutical Inc.3203dfc5-2cb1-4703-8d81-63fba07ddd982024-12-26WarningsExact identifier
application number: M001
unii: H0G9379FGK
Diphenhydramine HydrochlorideDIPHENHYDRAMINE HYDROCHLORIDERichmond Pharmaceuticals Inc.f184b2aa-91a4-44f9-b688-d4e3181819842024-12-26WarningsExact identifier
application number: M012
unii: TC2D6JAD40
Diphenhydramine HydrochlorideDIPHENHYDRAMINE HYDROCHLORIDERichmond Pharmaceuticals, Inc.2792032a-ff0f-4d5f-a8e3-b8b8c54f4e992024-12-26WarningsExact identifier
application number: M012
unii: TC2D6JAD40
Magnesium OxideMAGNESIUM OXIDERichmond Pharmaceuticals, Inc.9119b7f0-3e8a-7be7-e053-2995a90a46342024-12-26WarningsExact identifier
application number: M001

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.