Label: 70% ISOPROPYL ALCOHOL liquid
- NDC Code(s): 74793-0008-1
- Packager: Streamline Polymers LLC
- 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 September 24, 2020
If you are a consumer or patient please visit this version.
- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
When using this product keep out of eyes, do not inhale, do not apply over large areas of the body, do not use longer than 1 week.
Stop use and ask a doctor if condition persists or get worse.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- 16 oz NDC: 74793-0008-2
INGREDIENTS AND APPEARANCE
70% ISOPROPYL ALCOHOL
70% isopropyl alcohol liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74793-0008 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) 30 mL in 100 mL Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74793-0008-1 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/15/2020 Labeler - Streamline Polymers LLC (117054225) Registrant - Streamline Polymers LLC (117054225) Establishment Name Address ID/FEI Business Operations Streamline Polymers LLC 117054225 manufacture(74793-0008)