Label: MASK ON EVERY FACE VITAMIN E ALOE HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 52989-005-01, 52989-005-02, 52989-005-03, 52989-005-04, view more52989-005-05, 52989-005-06, 52989-005-07, 52989-005-08, 52989-005-09, 52989-005-10 - Packager: Taizhou Yadai Daily-Use Co., Ltd.
- 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 August 14, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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Warnings
For external use only. Flammable. Keep away from heat or flame
Do not use
- In children less than 2 months of age
- On open skin wounds
When using this product, keep out of eyes, ears or 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 serious condition.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MASK ON EVERY FACE VITAMIN E ALOE HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52989-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CARBOMER 940 (UNII: 4Q93RCW27E) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52989-005-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 2 NDC:52989-005-02 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 3 NDC:52989-005-03 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 4 NDC:52989-005-04 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 5 NDC:52989-005-05 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 6 NDC:52989-005-06 53 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 7 NDC:52989-005-07 75 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 8 NDC:52989-005-08 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 9 NDC:52989-005-09 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 10 NDC:52989-005-10 350 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/06/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/06/2020 Labeler - Taizhou Yadai Daily-Use Co., Ltd. (529899639) Establishment Name Address ID/FEI Business Operations Taizhou Yadai Daily-Use Co., Ltd. 529899639 manufacture(52989-005)