Label: 70% ISOPROPYL ALCOHOL- alcohol solution
- NDC Code(s): 67751-206-01
- Packager: Navajo Manufacturing Company Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Updated February 11, 2021
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- Active ingredient
For external use only.
Flammable. Keep away from fire or flame, heat, spark, electrical.
When using this product
- do not get into eyes
- do not inhale
- do not apply over large areas of the body
- do not use longer than 1 week
- Other information
- Inactive ingredient
- Questions or comments?
- Principal Display Panel
INGREDIENTS AND APPEARANCE
70% ISOPROPYL ALCOHOL
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67751-206 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67751-206-01 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/08/2020 Labeler - Navajo Manufacturing Company Inc. (091917799) Registrant - Navajo Manufacturing Company Inc. (136941411) Establishment Name Address ID/FEI Business Operations Marquis Extraction Technology LLC 117496233 label(67751-206) , manufacture(67751-206)