FDA.reportPublic FDA data

Aquation Anti-Chafe Cream

Manufacturer
RNA PHARMA, LLC
Effective date
2022-12-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:42

Label at a glance#

ProductAquation Anti-Chafe Cream
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredientsactive ingredients

INDICATIONS & USAGE SECTION

indications & usageindications & usage

DOSAGE & ADMINISTRATION SECTION

dosage & administrationdosage & administration

WARNINGS SECTION

warningswarnings

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

OTC - PURPOSE SECTION

purposepurpose

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label principalpackage label principal

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60717-730-042025-01-30C16284748780-12cef2736-8a19-d83d-e063-dadaa90ab31ff0d5f671-ccec-7a0b-e053-2a95a90a9e01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-730-04Aquation Anti-Chafe Cream113 g in 1 TUBELOTION1131
60717-730-04Aquation Anti-Chafe Cream1 in 1 BOXLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60717-730AQUATION ANTI-CHAFE CREAM (ZINC OXIDE) LOTION [RNA PHARMA, LLC]1Legacy NDC, 2 package rows20221229_f0d5f671-ccec-7a0b-e053-2a95a90a9e01.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-73060717-730-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
BENTONITEA3N5ZCN45CIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ZINC OXIDESOI2LOH54ZACTIB
WHITE PETROLATUMB6E5W8RQJ4IACT
SORBITAN OLIVATEMDL271E3GRIACT
SORBITAN MONOPALMITATE77K6Z421KUIACT
CERAMIDE 15THT33P7X7IACT
OATMEAL8PI54V663YIACT
XANTHAN GUMTTV12P4NEEIACT
CERAMIDE 2C04977SRJ5IACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
SUCROSE DISTEARATE33X4X4B90SIACT
CERAMIDE APF1X8L2B00JIACT
DIPROPYLENE GLYCOLE107L85C40IACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
CERAMIDE NP4370DF050BIACT
CERAMIDE 4SF3LP91341IACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CETEARYL OLIVATE58B69Q84JOIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
CETYL PALMITATE5ZA2S6B08XIACT
CHOLESTEROL97C5T2UQ7JIACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f0d5f671-cced-7a0b-e053-2a95a90a9e01f0d5f671-ccec-7a0b-e053-2a95a90a9e012022-12-27WarningsExact identifier
spl id: f0d5f671-cced-7a0b-e053-2a95a90a9e01
spl set id: f0d5f671-ccec-7a0b-e053-2a95a90a9e01

Reported adverse events (FAERS/openFDA)#

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