HAND SANITIZER- alcohol gel ningbo fareast industry co.,ltd Reference Label Set Id: a68674ba-455a-4d63-e053-2a95a90aed00 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. ---------- alcohol 75% v/v purpose :antiseptic alcohol 70% v/v purpose :antiseptic alcohol 60% v/v purpose :antiseptic to help reduce bacteria that potentially can cause disease.for use when soap and water are not available for external use only,flammable,keep away from heat or flame . in children less than 2 months of age .on open skin wounds when using this product keep out of eyes,ears,and mouth in case of contact with eyes,rinse eyes thorough 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 and ask a doctor if irriation 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 posion control center right away place enough product on hands to cover all surface,rub hands together until dry supervise children under 6 years when using this product to avoid swallowing package label principal dis play panel
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HAND SANITIZER- alcohol gel ningbo fareas t industry co.,ltdReference Label Set Id: a68674ba-455a-4d63-e053-2a95a90aed00 Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if theycomply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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alcohol 75% v/v purpose :antiseptic
alcohol 70% v/v purpose :antiseptic
alcohol 60% v/v purpose :antiseptic
to help reduce bacteria that potentially can cause disease.for use when soap and water are not available
for external use only,flammable,keep away from heat or flame
. in children less than 2 months of age
.on open skin wounds
when using this product keep out of eyes,ears,and mouth in case of contact with eyes,rinse eyesthorough 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 rightaway.
stop use and ask a doctor if irriation 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 posion control center rightaway
place enough product on hands to cover all surface,rub hands together until dry supervise children under 6 years when using this product to avoid swallowing
package label principal display panel
75% alcohol concent
1000ml NDC: 78623-375-01
500ml NDC: 78623-375-02
237ml NDC: 78623-375-03
100ml NDC: 78623-375-04
60ml NDC: 78623-375-05
30ml NDC: 78623-375-06
70% alcohol concent
1000ml NDC: 78623-370-01
500ml NDC: 78623-370-02
237ml NDC: 78623-370-03
100ml NDC: 78623-370-04
60ml NDC: 78623-370-05
30ml NDC: 78623-370-06
60% alcohol concent
1000ml NDC: 78623-360-01
500ml NDC: 78623-360-02
237ml NDC: 78623-360-03
100ml NDC: 78623-360-04
60ml NDC: 78623-360-05
30ml NDC: 78623-360-06
HAND SANITIZER alcohol gel
Product InformationProduct T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:78 6 23-370
Route of Adminis tration TOPICAL
Active Ingredient/Active MoietyIngredient Name Basis o f Strength Strength
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M) ALCOHOL 70 mL in 10 0 mL
Inactive IngredientsIngredient Name Strength
WATER (UNII: 0 59 QF0 KO0 R)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
HYDRO GEN PERO XIDE (UNII: BBX0 6 0 AN9 V)
GLYCERIN (UNII: PDC6 A3C0 OX)
CARBO XYPO LYMETHYLENE (UNII: 0 A5MM30 7FC)
Packaging# Item Code Package Description Marketing Start Date Marketing End Date1 NDC:78 6 23-370 -0 1 10 0 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
2 NDC:78 6 23-370 -0 2 50 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
3 NDC:78 6 23-370 -0 3 237 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
4 NDC:78 6 23-370 -0 4 10 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
5 NDC:78 6 23-370 -0 5 6 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
6 NDC:78 6 23-370 -0 6 30 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
Marketing InformationMarke ting Cate gory Application Numbe r or Monograph Citation Marke ting Start Date Marke ting End Date
OTC mo no graph no t fina l part333A 12/31/20 20
HAND SANITIZER alcohol gel
Product InformationProduct T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:78 6 23-375
Route of Adminis tration TOPICAL
Active Ingredient/Active MoietyIngredient Name Basis o f Strength Strength
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M) ALCOHOL 75 mL in 10 0 mL
Inactive IngredientsIngredient Name Strength
CARBO XYPO LYMETHYLENE (UNII: 0 A5MM30 7FC)
WATER (UNII: 0 59 QF0 KO0 R)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
GLYCERIN (UNII: PDC6 A3C0 OX)
HYDRO GEN PERO XIDE (UNII: BBX0 6 0 AN9 V)
Packaging# Item Code Package Description Marketing Start Date Marketing End Date1 NDC:78 6 23-375-0 1 10 0 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
2 NDC:78 6 23-375-0 2 50 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
3 NDC:78 6 23-375-0 3 237 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
4 NDC:78 6 23-375-0 4 10 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
5 NDC:78 6 23-375-0 5 6 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
6 NDC:78 6 23-375-0 6 30 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
Marketing InformationMarke ting Cate gory Application Numbe r or Monograph Citation Marke ting Start Date Marke ting End Date
OTC mo no graph no t fina l part333A 0 1/0 4/20 21
HAND SANITIZER alcohol gel
Product InformationProduct T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:78 6 23-36 0
Route of Adminis tration TOPICAL
ningbo fareast industry co.,ltd
Active Ingredient/Active MoietyIngredient Name Basis o f Strength Strength
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M) ALCOHOL 75 mL in 10 0 mL
Inactive IngredientsIngredient Name Strength
GLYCERIN (UNII: PDC6 A3C0 OX)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
HYDRO GEN PERO XIDE (UNII: BBX0 6 0 AN9 V)
CARBO XYPO LYMETHYLENE (UNII: 0 A5MM30 7FC)
WATER (UNII: 0 59 QF0 KO0 R)
Packaging# Item Code Package Description Marketing Start Date Marketing End Date1 NDC:78 6 23-36 0 -0 1 10 0 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
2 NDC:78 6 23-36 0 -0 2 50 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
3 NDC:78 6 23-36 0 -0 3 237 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
4 NDC:78 6 23-36 0 -0 4 10 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
5 NDC:78 6 23-36 0 -0 5 6 0 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
6 NDC:78 6 23-36 0 -0 6 30 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct 0 1/0 4/20 21
Marketing InformationMarke ting Cate gory Application Numbe r or Monograph Citation Marke ting Start Date Marke ting End Date
OTC mo no graph no t fina l part333A 0 1/0 4/20 21
Labeler - ningbo fareas t indus try co.,ltd (554535808)