NDC 00591-0810 - Silver Sulfadiazine

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 00591-0810
Manufacturer: Keltman Pharmaceuticals Inc. | Sandhills Packaging
Effective date: 2010-09-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Silver Sulfadiazine - Keltman Pharmaceuticals Inc. \| Sandhills Packaging	Keltman Pharmaceuticals Inc. \| Sandhills Packaging	2010-09-22	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SILVER SULFADIAZINE	ACTIVE INGREDIENT	W46JY43EJR	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
SILVER SULFADIAZINE	ACTIVE MOIETY	W46JY43EJR	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
CETYL ALCOHOL	INACTIVE INGREDIENT	936JST6JCN	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
ISOPROPYL MYRISTATE	INACTIVE INGREDIENT	0RE8K4LNJS	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
POLYOXYL 40 STEARATE	INACTIVE INGREDIENT	13A4J4NH9I	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
SORBITAN MONOOLEATE	INACTIVE INGREDIENT	06XEA2VD56	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
STEARYL ALCOHOL	INACTIVE INGREDIENT	2KR89I4H1Y	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	SILVER SULFADIAZINE CREAM [KELTMAN PHARMACEUTICALS INC.]	2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 40 of 40 · 789 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Homeoplex D	GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,	Supplement Clinic, LLC.	cd6b48ab-3566-484d-8deb-15ef6f8e7e8f	2017-11-01	Warnings	Exact identifier unii: 4T6H12BN9U unii: 2KR89I4H1Y
Sterile Water	WATER	Baxter Healthcare Corporation	ef3e79c5-3f58-4b36-a296-64b7d9a651c1	2017-10-17	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
CVS Health Original SPF 15 Lip Balm	OXYBENZONE, OCTINOXATE, PETROLATUM	CVS	6d58a18c-62ba-4cee-b3cc-51db746ba50e	2016-09-14	Warnings	Exact identifier unii: 4T6H12BN9U
CVS Health Cherry SPF 15 Lip Balm	OXYBENZONE, OCTINOXATE, PETROLATUM	CVS	84a621fe-890e-4c88-9f26-f013c32b52b7	2016-09-14	Warnings	Exact identifier unii: 4T6H12BN9U
CVS Health Cherry SPF 15 Lip Balm	OXYBENZONE, OCTINOXATE, PETROLATUM	CVS	bfbf0241-51a6-4d9d-bee1-741d1645037d	2016-09-14	Warnings	Exact identifier unii: 4T6H12BN9U
CVS Health Original SPF 15 Lip Balm	OXYBENZONE, OCTINOXATE, PETROLATUM	CVS	e49680bd-bd61-40cf-abc8-51a1c8808726	2016-09-14	Warnings	Exact identifier unii: 4T6H12BN9U
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
36c67b60-9529-4f19-a4b8-b68788f836c1			27c5999a-0bbe-4d20-9a9e-3546c8189ae3	2010-09-22	Warnings, Adverse reactions	Exact identifier spl id: 36c67b60-9529-4f19-a4b8-b68788f836c1 spl set id: 27c5999a-0bbe-4d20-9a9e-3546c8189ae3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.