Active Ingredient
Aluminum chlorohydrate 12%
Kiehls Since 1851 Body Fuel Antiperspirant And Deodorant Lotion
FDA Label NDC 49967-639
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by L'oreal Usa Products Inc for the product Kiehls Since 1851 Body Fuel Antiperspirant And Deodorant (NDC 49967-639). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, stop use if, ask a doctor before use if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
reduces underarm wetness
Warnings
For external use only
Do Not Use
on broken skin
Stop Use If
rash or irritation occurs
Ask A Doctor Before Use If
you have kidney disease
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
apply to underarms only
Inactive Ingredients
water, cetearyl alcohol, fragrance, ceteareth-33, perlite, dimethicone, phenoxyethanol, pentylene glycol, limonene, caffeine, tocopheryl acetate, zinc gluconate, ascorbyl glucoside, linalool, citral
Package Label.Principal Display Panel
Image Of A Carton (Kiehlsbodyfuelap)
Image Of A Bottle (Kiehlsbodyfuelapbot)
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