Maxim FDF: Package Insert and Label Information

MAXIM FDF- chloroxylenol soap
Midlab Incorporated

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Principal
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Active
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Purpose
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Uses
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Warnings
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Ask Doctor
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KOOROC
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Dosage and Admin
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Inactive Ingredients
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MAXIM FDF
pcmx, hand soap soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70542-201
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL 0.1 g in 1 L
Inactive Ingredients
Ingredient Name Strength
SODIUM LAURETH SULFATE
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE
LAURAMINE OXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70542-201-41 3.78 L in 1 BOTTLE, PLASTIC None
2 NDC:70542-201-55 208 L in 1 DRUM None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 03/11/2019
Labeler — Midlab Incorporated (047371463)
Registrant — Midlab Incorporated (047371463)
Establishment
Name Address ID/FEI Operations
Midlab Incorporated 047371463 manufacture (70542-201)

Revised: 05/2021 Midlab Incorporated

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