Label: EGOLAN- ethyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75448-026-01, 75448-026-02, 75448-026-03, 75448-026-04, view more75448-026-05, 75448-026-06, 75448-026-07 - Packager: Sanrace Biotechnology Co., Ltd.
- 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 August 4, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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- Other information
- Inactive Ingredients
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SPL UNCLASSIFIED SECTION
KILLS 99.9% OF GERMS
ALOE VERA SOOTHING GEL
70% ALCOHOL
STAY SAFE
Keep your hands clean on the go with Alchemy Living 2 Pc Hand Sanitizer set. Helps reduce bacteria on
the skin while leaving hands feeling smooth.
Manufacturer: Sanrace Biotechnology Co.,Ltd.
Address: 268 Yanzhou Road, Lanxi Economic Development Zone, Zhejiang Province.
Made in China
- Packaging
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INGREDIENTS AND APPEARANCE
EGOLAN
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75448-026 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) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ALOE VERA LEAF (UNII: ZY81Z83H0X) TROLAMINE (UNII: 9O3K93S3TK) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75448-026-03 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2020 2 NDC:75448-026-04 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2020 3 NDC:75448-026-05 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2020 4 NDC:75448-026-06 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2020 5 NDC:75448-026-07 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2020 6 NDC:75448-026-02 2 in 1 BLISTER PACK 08/01/2020 6 NDC:75448-026-07 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 7 NDC:75448-026-01 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/01/2020 Labeler - Sanrace Biotechnology Co., Ltd. (543000938) Establishment Name Address ID/FEI Business Operations Sanrace Biotechnology Co., Ltd. 543000938 manufacture(75448-026)