DailyMed - 4129 FIRST AID KIT kit

NDC Code(s): 0498-0011-77, 0498-0121-00, 0498-0143-04, 0498-0501-00, view more
0498-0733-00, 0498-0800-34, 0498-3334-00, 0498-4129-01
Packager: Honeywell Safety Products USA, INC

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 23, 2021

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Ammonia Active ingredient

Ammonia 15%
Ammonia Purpose

Respiratory stimulant
Ammonia Uses
- to prevent or treat fainting
Ammonia Warnings
For external use only
Do not use
- if you have breathing problems such as asthma or emphysema
Stop use and ask a doctor if
- condition persists
Keep out of reach of children
- If swallowed get medical help or contact a Poison Control Center right away.
Ammonia Directions
- hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve.
- hold near nostrils for inhalation of volatile vapor
Ammonia Other information
- store at room temperature away from light
Ammonia Inactive ingredient

alcohol USP, FD&C red #40, lavender oil, lemon oil fcc, nutmeg oil, purified water
Ammonia Questions or Comments?

1-800-430-5490
Pyrocaine Active ingredient

Benzocaine 20%

Benzethonium chloride 0.2%
Pyrocaine Purpose

Topical anesthetic

Topical antiseptic
Pyrocaine Uses
For the temporary relief of pain and itching, and to help protect against skin infection in:
- minor burns
- minor skin irritations
- minor cuts and scrapes
- insect bites
- sunburns
Do not use
- in or near the eyes or over large portions of the body
- in case of deep or puncture wounds or on:
- raw surfaces
- blistered areas
- animal bites
- serious burns
Keep out of reach of children
- If swallowed, get medical help or contact a Poison Control Center right away
Pyrocaine Warnings
For external use only

Flammable
- keep away from fire or flame
- contents under pressure
- do not puncture, incinerate or expose container to temperatures above 120 o F
Stop use and ask a doctor if
- If condition persists or worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
Pyrocaine Directions
- clean the affected area
- shake can well before using
- hold can 6 to 12 inches away from the affected area and spray liberally
- apply to affected area not more than 3 times daily
- for adult institutional use only
- not intended for use on children
Pyrocaine Other information
- avoid inhaling
- use only as directed
- intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal
Pyrocaine Inactive ingredients

butane,dipropylene glycol, isobutane, propane
PVP Active ingredient

Povidone-iodine 10%

(equivalent to 1% titratable iodine)
PVP Purpose

First aid antiseptic
PVP Uses
- first aid antiseptic to help prevent infection in minor cuts, scrapes and burns
PVP Warnings
For external use only.
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
Stop use and ask a doctor if
- condition worsens or persists for more than 72 hours
- irritation and redness develops
Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.
PVP Directions
- clean the affected area
- apply1 to 3 times daily
- may be covered with a sterile bandage
- if bandaged, let dry first
- discard wipe after single use
PVP Other information
- do not use on individuals who are allergic or sensitive to iodine
- store at controlled temperature 59-86ºF (15-30ºC)
- do not use if pouch is open or torn
PVP Inactive ingredients

nonoxynol 9, water
PVP Questions

1-800-430-5490
Sting Relief Active ingredient (in each wipe)

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%
Sting Relief Purpose

Antiseptic

Topical pain relief
Sting Relef Uses
- prevent infection in minor scrapes, and temporary relief of itching of insect bites
Sting Relief Warnings
For external use only

Flammable, keep away from open fire or flame
Do not use
- over large areas of the body
- in eyes
- over raw or blistered areas
Stop use and ask a doctor
- if conditions worsen or persist for more than 7 days or clear up and occur again within a few days
Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.
Sting Relief Directions
- adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
- children under 2 years of age: consult a doctor.
Sting Relief Inactive ingredients

benzalkonium chloride, menthol, and purified water
Sting Relief Questions or Comments?

1-800-430-5490
alcohol Active ingredient

Isopropyl alcohol 70%
Alcohol Purpose

First aid antiseptic
Alcohol Uses
- first aid to help prevent infection in minor cuts, scrapes, and burnsv
Alcohol Warnings
For external use only

Flammable, keep away from fire and flame
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
When using this product
- do not use longer than 1 week unless directed by a doctor
Stop use and consult a doctor if
- condition persists or gets worse
Keep out of the reach of children
- If swallowed, get medical help or contact a Poison Control center right away
Alcohol Directions
- clean the affected area
- may be covered with a sterile bandage
- apply wipe to affeted are 1 to 3 times daily
- discard wipe after single use
Alcohol Other information
- store at room temperature 15 0 to 25 0 C (59 0 to 77 0 F)
- do not use if packet is torn or opened
Alcohol Inactive ingredient

water
Alcojol Questions

1-800-430-5490
Hydrocortisone Active ingredient (in each gram)

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)
Hydrocortisone Purpose

Anti-itch cream
Hydrocortisone Uses
- for the temporary relief of itching associated with minor skin irritations and rashes
Hydrocortisone Warnings
For external use only
Ask a doctor before use
- if you are using any other hydrocortisone product
When using the product
- avoid contact with eyes
- do not begin use of any other hydrocortisone product unless you have consulted a doctor
- do not use for the treatment of diaper rash
Stop use and ask a doctor if
- condition worsens
- condition persists for more than 7 days
- condition clears up and recurs within a few days
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.
Hydrocortisone Directions
- adults and children 2 years and older:
- clean the affected area
- apply to the area not more than 3 to 4 times daily
- children under 2 years of age: consult a doctor
Hydrocortisone Other information
- store at room temperature (do not freeze)
Hydrocortisone Inactive ingredients

cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, trolamine
Hydrocortisone Questions or comments?

1-800-430-5490
BZK Active ingredient

Benzalkonium chloride 0.13% w/v
BZK Purpose

First aid antiseptic
BZK Uses

Antiseptic cleansing of face, hands, and body without soap and water
BZK Warnings
For external use only
Do not use
- in the eyes or over large areas of the body
- on mucous membranes
- on irritated skin
- in case of deep puncture wounds, animal bites or serious burns, consult a doctor
- longer than 1 week unless directed by a doctor
Stop use and ask a doctor if
- if irritation, redness or other symptoms develop
- the condition persists or gets worse
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.
BZK Directions
- tear open packet and use as a washcloth
BZK Other information
- store at room temperature 15 0 to 30 0 C (59 0 - 86 0 F)
- do not reuse towelette
BZK Inactive ingredient

water
BZK Questions

1-800-430-5490
4129 SF00004226 Kit Contents

1 AMMONIA INHALANTS 10 PER

1 EYE DRESS PKT W/4 ADH STRIPS

1 TRIANGULAR BDG, NON-STERILE

1 INSTANT COLD PACK 4" X 6"

1 ALCOHOL PREP PADS 10P

1 HYDROCORTISON,1.O%,1/32 OZ,10P

1 RESPONSE KIT BLOODBORNE PATHOG

1 SCISSOR BDGE 4" RED PLS HDL

1 BANDAGE COMP 2" W/TELFA PAD 4

1 BANDAGE COMP 4" W/TELFA PAD 1

LBL STOCK 6-3/8"X4"

LBL STOCK 4"X2-7/8"

1 LBL STOCK 3"x1-7/8"

1 PR LRG NITRILE GLVES ZIP BAG

1 1" X 3" PLASTIC BANDS 16/BAG

1 KIT STL 24 UN WHITE 01

1 PVP IODINE SWABS 10

1 STING Relief SWAB 10

1 PYRO-CAINE AERO 2/BX

1 RED BIO BAGS 2/BX

1 FACE MASK/EYE SHIELD

1 LIQD TRTMNT SYS 1 EA

1 DISP. TOWEL/WIPES 2EA

1 IMPERVIOUS GOWN 1 EA
Ammonia Principal Display Panel
Pyrocaine Principal Display Panel
PVP Principal Display Panel
Sting Relief Principal Display Panel
Alcohol Principal Display Panel
Hydrocortisone Principal Display Panel
BZK Principal Display Panel
4129 Kit Label SF00004226

INGREDIENTS AND APPEARANCE

4129 FIRST AID KIT
4129 first aid kit kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0498-4129

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-4129-01	1 in 1 KIT; Type 0: Not a Combination Product	10/18/2018

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	10 PACKET	9 g
Part 2	10 AMPULE	3 mL
Part 3	2 CAN	28.4 g
Part 4	10 POUCH	4 mL
Part 5	10 POUCH	3 mL
Part 6	4 PACKET	5.6 mL
Part 7	10 POUCH	4 mL
Part 8	10 PACKET	9 g

Part 1 of 8

HYDROCORTISONE
anti-itch cream

Product Information
Item Code (Source)	NDC:0498-0801
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
LIGHT MINERAL OIL (UNII: N6K5787QVP)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	03/06/2013

Part 2 of 8

AMMONIA INHALENT
ammonia inhalent inhalant

Product Information
Item Code (Source)	NDC:0498-3334
Route of Administration	RESPIRATORY (INHALATION)

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	0.045 g in 0.3 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-3334-00	0.3 mL in 1 AMPULE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/18/2018

Part 3 of 8

PYROCAINE BURN
benzocaine, benzethonium chloride aerosol, spray

Product Information
Item Code (Source)	NDC:0498-0011
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	20 g in 100 g
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
1,1,3-TRI(3-TERT-BUTYL-4-HYDROXY-6-METHYLPHENYL)BUTANE (UNII: BF6E9O0XJN)
ISOBUTANE (UNII: BXR49TP611)
1,1,3-TRIS(2-CHLOROETHOXY)PROPANE (UNII: 4FEX9N888E)
DIPROPYLENE GLYCOL (UNII: E107L85C40)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0011-77	14.2 g in 1 CAN; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	01/01/2018

Part 4 of 8

STING RELIEF PAD
ethyl alcohol, lidocaine swab

Product Information
Item Code (Source)	NDC:0498-0733
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.5 mL in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
MENTHOL (UNII: L7T10EIP3A)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0733-00	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	12/23/2017

Part 5 of 8

PVP IODINE WIPE
povidone-iodine 10% swab

Product Information
Item Code (Source)	NDC:0498-0121
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
NONOXYNOL-9 (UNII: 48Q180SH9T)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0121-00	0.3 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		09/18/2018

Part 6 of 8

ANTISEPTIC TOWELETTE
benzalkonium chloride liquid

Product Information
Item Code (Source)	NDC:0498-0501
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0501-00	1.4 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	12/21/2017

Part 7 of 8

ALCOHOL WIPE
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC:0498-0143
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0143-04	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	09/18/2018

Part 8 of 8

HYDROCORTISONE
anti-itch cream ointment

Product Information
Item Code (Source)	NDC:0498-0800
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
LIGHT MINERAL OIL (UNII: N6K5787QVP)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0498-0800-34	0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	03/06/2013	10/15/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		10/18/2018

Labeler - Honeywell Safety Products USA, INC (079287321)

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Published Date (What is this?)	Version	Files
Dec 24, 2021	4 (current)	download
Oct 17, 2019	2	download
May 13, 2019	1	download

	RxCUI	RxNorm NAME	RxTTY
1	797544	isopropyl alcohol 70 % Medicated Pad	PSN
2	797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD
3	797544	isopropyl alcohol 70 % Medicated Pad	SY
4	797544	isopropyl alcohol 70 % Topical Cloth	SY
5	797544	isopropyl alcohol 70 % Topical Swab	SY
6	1038558	benzalkonium chloride 0.13 % Medicated Pad	PSN
7	1038558	benzalkonium chloride 1.3 MG/ML Medicated Pad	SCD
8	1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Patch	SY
9	1038558	benzalkonium chloride 0.13 GM per 100 GM Topical Swab	SY
10	1038558	benzalkonium chloride 0.13 % Topical Swab	SY
11	1038558	benzalkonium chloride 1 ML per 750 ML Topical Swab	SY
12	1043690	hydrocortisone acetate 1 % Topical Cream	PSN
13	1043690	hydrocortisone acetate 10 MG/ML Topical Cream	SCD
14	1043690	hydrocortisone acetate 1 % Topical Cream	SY
15	1049108	benzethonium Cl 0.2 % / benzocaine 20 % Topical Spray	PSN
16	1049108	benzethonium chloride 2 MG/ML / benzocaine 200 MG/ML Topical Spray	SCD
17	1049108	benzethonium Cl 0.2 % / benzocaine 20 % Topical Spray	SY
18	1190560	ethanol 50 % / lidocaine HCl 2 % Medicated Pad	PSN
19	1190560	ethanol 0.5 ML/ML / lidocaine hydrochloride 20 MG/ML Medicated Pad	SCD
20	1190560	ethanol 50 % / lidocaine hydrochloride 2 % Medicated Pad	SY
21	1299889	ammonia 15 % Nasal Inhalant	PSN
22	1299889	ammonia 150 MG/ML Nasal Inhalant	SCD
23	1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY
24	1299889	ammonia 0.3 ML Nasal Inhalant	SY
25	1299889	ammonia 15 % Nasal Inhalant	SY
26	1440184	hydrocortisone acetate 1 % Topical Ointment	PSN
27	1440184	hydrocortisone acetate 0.01 MG/MG Topical Ointment	SCD
28	1440184	hydrocortisone acetate 1 % Topical Ointment	SY

Label: 4129 FIRST AID KIT kit

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Drug Label Information

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Keep out of reach of children

Stop use and ask a doctor if

Ask a doctor before use if you have

Stop use and ask a doctor if

Keep out of reach of children.

Do not use

Stop use and ask a doctor

Keep out of reach of children.

Ask a doctor before use if you have

When using this product

Stop use and consult a doctor if

Keep out of the reach of children

Ask a doctor before use

When using the product

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Find additional resources

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More Info on this Drug

	NDC
1	0498-0011-77
2	0498-0121-00
3	0498-0143-04
4	0498-0501-00
5	0498-0733-00
6	0498-0800-34
7	0498-3334-00
8	0498-4129-01

Label: 4129 FIRST AID KIT kit

View Package Photos

VIEW MORE

Drug Label Info

Safety

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More Info For This Drug

Drug Label Information

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Keep out of reach of children

Stop use and ask a doctor if

Ask a doctor before use if you have

Stop use and ask a doctor if

Keep out of reach of children.

Do not use

Stop use and ask a doctor

Keep out of reach of children.

Ask a doctor before use if you have

When using this product

Stop use and consult a doctor if

Keep out of the reach of children

Ask a doctor before use

When using the product

Stop use and ask a doctor if

Keep out of reach of children

Do not use

Stop use and ask a doctor if

Keep out of reach of children

Find additional resources

Safety

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More Info on this Drug

4129 FIRST AID KIT kit

Number of versions: 3

4129 FIRST AID KIT kit

4129 FIRST AID KIT kit

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4129 FIRST AID KIT kit

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