Label: SANI CLEAN PLUS- isopropyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 90082-970-02, 90082-970-04, 90082-970-08, 90082-970-12, view more90082-970-16, 90082-970-32, 90082-970-67 - Packager: First Galaxy Enterprises 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.
Drug Label Information
Updated October 22, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTION
This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:
- Isopropyl Alcohol (75%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
- Glycerol (1.45% v/v).
- Hydrogen peroxide (0.125% v/v).
- Sterile distilled water or boiled cold water.
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
SANI CLEAN PLUS
isopropyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:90082-970 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength CITRUS FRUIT (UNII: XDK00Z8012) WATER (UNII: 059QF0KO0R) ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:90082-970-02 59 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 2 NDC:90082-970-04 118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 3 NDC:90082-970-08 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 4 NDC:90082-970-16 473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 5 NDC:90082-970-32 946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 6 NDC:90082-970-67 1981 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 7 NDC:90082-970-12 3785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/11/2020 Labeler - First Galaxy Enterprises Inc (114966288) Establishment Name Address ID/FEI Business Operations HPPE LLC 078769356 manufacture(90082-970)