DailyMed - KEW HAND SANITISER SUMMER ROSE- alcohol spray KEW HAND SANITISER PINEAPPLE AND PINK LOTUS- alcohol spray KEW HAND SANITISER NARCISSUS LIME- alcohol spray KEW HAND SANITISER GRAPEFRUIT AND LILY- alcohol spray KEW HAND SANITISER BLUEBELL AND JASMINE- alcohol spray KEW HAND SANITISER MAGNOLIA AND PEAR- alcohol spray KEW HAND SANITISER FIG AND GRAPE- alcohol spray KEW HAND SANITISER IRIS- alcohol spray KEW HAND SANITISER MANGO- alcohol spray KEW HAND SANITISER LAVENDER AND ROSEMARY- alcohol spray KEW HAND SANITISER BERGAMOT AND GINGER- alcohol spray KEW HAND SANITISER COCONUT- alcohol spray KEW HAND SANITISER LEMONGRASS AND LIME- alcohol spray KEW HAND SANITISER SANDALWOOD AND PINK PEPPER- alcohol spray KEW HAND SANITISER ELDERFLOWER AND POMELO- alcohol spray KEW HAND SANITISER OSMANTHUS ROSE- alcohol spray KEW HAND SANITISER JASMINE PEACH- alcohol spray

Contains inactivated NDC Code(s)
NDC Code(s): 81318-001-01, 81318-002-01, 81318-003-01, 81318-004-01, view more
81318-005-01, 81318-006-01, 81318-007-01, 81318-008-01, 81318-009-01, 81318-010-01, 81318-011-01, 81318-012-01, 81318-013-01, 81318-014-01, 81318-015-01, 81318-016-01, 81318-017-01
Packager: Christina May 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 January 4, 2021

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)

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Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic
Purpose

Antiseptic, Hand Sanitizer
Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
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

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

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients

Aqua, glycerin, parfum, tocopheryl acetate, aloe barbadensis juice powder
Package Label - Principal Display Panel NDC: 81318-001-01

100 mL NDC: 81318-001-01
Package Label - Principal Display Panel NDC: 81318-002-01

100mL NDC: 81318-002-01
Package Label - Principal Display Panel NDC: 81318-003-01

100mL NDC: 81318-003-01
Package Label - Principal Display Panel NDC: 81318-004-01

100mL NDC: 81318-004-01
Package Label - Principal Display Panel NDC: 81318-005-01

100mL NDC: 81318-005-01
Package Label - Principal Display Panel NDC: 81318-006-01

100mL NDC: 81318-006-01
Package Label - Principal Display Panel NDC: 81318-007-01

100mL NDC: 81318-007-01
Package Label - Principal Display Panel NDC: 81318-008-01

100mL NDC: 81318-008-01
Package Label - Principal Display Panel NDC: 81318-009-01

100mL NDC: 81318-009-01
Package Label - Principal Display Panel NDC: 81318-010-01

100mL NDC: 81318-010-01
Package Label - Principal Display Panel NDC: 81318-011-01

100mL NDC: 81318-011-01
Package Label - Principal Display Panel NDC: 81318-012-01

100mL NDC: 81318-012-01
Package Label - Principal Display Panel NDC: 81318-013-01

100mL NDC: 81318-013-01
Package Label - Principal Display Panel NDC: 81318-014-01

100mL NDC: 81318-014-01
Package Label - Principal Display Panel NDC: 81318-015-01

100mL NDC: 81318-015-01
Package Label - Principal Display Panel NDC: 81318-016-01

100mL NDC: 81318-016-01
Package Label - Principal Display Panel NDC: 81318-017-01

100mL NDC: 81318-017-01

INGREDIENTS AND APPEARANCE

KEW HAND SANITISER SUMMER ROSE
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-002-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER PINEAPPLE AND PINK LOTUS
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-014
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-014-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER NARCISSUS LIME
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-015
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-015-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER GRAPEFRUIT AND LILY
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-003
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-003-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER BLUEBELL AND JASMINE
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-007-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER MAGNOLIA AND PEAR
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-009
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-009-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER FIG AND GRAPE
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-010
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-010-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER IRIS
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-011
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-011-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER MANGO
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-012
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-012-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER LAVENDER AND ROSEMARY
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-001-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER BERGAMOT AND GINGER
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-008
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-008-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER COCONUT
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-013
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-013-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER LEMONGRASS AND LIME
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-004
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-004-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER SANDALWOOD AND PINK PEPPER
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-005
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-005-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER ELDERFLOWER AND POMELO
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-006
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-006-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER OSMANTHUS ROSE
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-016
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-016-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

KEW HAND SANITISER JASMINE PEACH
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81318-017
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	78 mL in 78 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81318-017-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/04/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/04/2021

Labeler - Christina May Ltd (215632780)

Registrant - Christina May Ltd (215632780)

Name	Address	ID/FEI	Business Operations
Establishment
Christina May Ltd		215632780	manufacture(81318-001, 81318-002, 81318-003, 81318-004, 81318-005, 81318-006, 81318-007, 81318-008, 81318-009, 81318-010, 81318-011, 81318-012, 81318-013, 81318-014, 81318-015, 81318-016, 81318-017)

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	NDC
1	81318-001-01 (inactivated)
2	81318-002-01 (inactivated)
3	81318-003-01 (inactivated)
4	81318-004-01 (inactivated)
5	81318-005-01 (inactivated)
6	81318-006-01 (inactivated)
7	81318-007-01 (inactivated)
8	81318-008-01 (inactivated)
9	81318-009-01 (inactivated)
10	81318-010-01 (inactivated)
11	81318-011-01 (inactivated)
12	81318-012-01 (inactivated)
13	81318-013-01 (inactivated)
14	81318-014-01 (inactivated)
15	81318-015-01 (inactivated)
16	81318-016-01 (inactivated)
17	81318-017-01 (inactivated)

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If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.