Label: DERMONANO- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75751-070-04, 75751-070-16, 75751-070-26 - Packager: PGH LABORATORIOS DO BRASIL LTDA.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated May 12, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or Comments
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Principal Display Panel
NDC: 75751-070-04
Gel 70% (alcohol) - Read Instructions before use contains Hydrated Ethyl Alcohol 70 INPM
Gel 70% (alcohol)
Sanitation Effective against bacteria and germs
Requires no water
Danger: Flammable
Keep out of reach of children
Keep away from fire or flame
For external use only
See other cautions on opposite panel of label
Net Wt. 120g e 4.2 oz
NDC: 75751-070-16
Gel 70% (alcohol) - Read Instructions before use contains Hydrated Ethyl Alcohol 70 INPM
Gel 70% (alcohol)
Sanitation Effective against bacteria and germs
Requires no water
Danger: Flammable
Keep out of reach of children
Keep away from fire or flame
For external use only
See other cautions on opposite panel of label
Gel 70% (alcohol)
Net Wt. 480g e 16.9 oz
NDC: 75751-070-26
Gel 70% (alcohol) - Read Instructions before use contains Hydrated Ethyl Alcohol 70 INPM
Gel 70% (alcohol)
Sanitation Effective against bacteria and germs
Requires no water
Danger: Flammable
Keep out of reach of children
Keep away from fire or flame
For external use only
See other cautions on opposite panel of label
Gel 70% (alcohol)
Net Wt. 1000L e 33814oz
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INGREDIENTS AND APPEARANCE
DERMONANO
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75751-070 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ISOPROPYL ALCOHOL (UNII: ND2M416302) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) PANTHENOL (UNII: WV9CM0O67Z) TRIISOPROPANOLAMINE (UNII: W9EN9DLM98) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75751-070-04 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 2 NDC:75751-070-16 480 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 3 NDC:75751-070-26 1000000 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/11/2020 Labeler - PGH LABORATORIOS DO BRASIL LTDA. (903309948) Registrant - PGH LABORATORIOS DO BRASIL LTDA. (903309948)